Chemistry 5 Revision Flashcards

1
Q

Acid hydrolysis of nitriles

A

Heated under reflux with dilute acid, produce carboxylic acid and salt

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2
Q

Hypochlorous acid (HOCl) can indeed decompose in the presence of sunlight,

A

Hypochlorous acid (HOCl) can indeed decompose in the presence of sunlight, particularly when exposed to ultraviolet (UV) radiation. The decomposition of HOCl can result in the formation of other compounds, such as oxygen (O2) and hydrogen chloride (HCl). This process is often accelerated in the presence of certain catalysts or under specific environmental conditions. The decomposition of HOCl plays a role in various chemical and biological processes, including water treatment, disinfection, and atmospheric chemistry.

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3
Q

Oil drop experiment

A

The “oil drop experiment” is attributed to American physicist Robert A. Millikan, not “Milkman.” This experiment was conducted in 1909 and was designed to determine the fundamental unit of electric charge, known as the electron charge ().

In the oil drop experiment, Millikan observed the motion of tiny oil droplets suspended in a chamber filled with air. By applying an electric field to the chamber, Millikan was able to manipulate the motion of the oil droplets. By carefully measuring the electric field strength required to balance the gravitational force acting on the droplets, Millikan was able to determine the magnitude of the electric charge on each droplet.

Through meticulous experimentation and analysis, Millikan determined that the electric charge on each droplet was a multiple of a fundamental unit of charge, which we now know as the electron charge (). He measured the charge on multiple droplets and found that the charges were all integer multiples of a certain value, which he determined to be approximately coulombs, the charge of a single electron.

Therefore, the oil drop experiment provided strong experimental evidence for the quantization of electric charge and enabled Millikan to determine the value of the electron charge with remarkable precision.

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4
Q

Change in heat is less than zero

A

Exothermic

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5
Q

In industrial production of hydrogen from natural gas, CO2 produced is collected by

A

Washing under pressure

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6
Q

Potassium dichromate (( \text{K}_2\text{Cr}_2\text{O}_7 )) is commonly used as an oxidizing agent in various chemical reactions

A

and is often used as an indicator in titrations. It is orange-red in color.When certain gases are introduced into a solution of potassium dichromate, they can undergo redox reactions with the dichromate ion (( \text{Cr}_2\text{O}_7^{2-} )), causing it to change color. Some gases that can cause such color changes include:Sulfur dioxide (SO2): Sulfur dioxide can reduce potassium dichromate to chromium(III) ions (( \text{Cr}^{3+} )), causing the orange-red color of potassium dichromate to change to green as chromium(III) ions are green in solution.Hydrogen sulfide (H2S): Hydrogen sulfide can also reduce potassium dichromate to chromium(III) ions, resulting in the same green color change.Carbon monoxide (CO): Carbon monoxide can reduce potassium dichromate to chromium(III) ions as well, causing the solution to change to a green color.These are just a few examples of gases that can change the color of potassium dichromate solution. The specific color change observed will depend on the concentration of the potassium dichromate solution, the concentration of the gas, and the reaction conditions.

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7
Q

Limestone (calcium carbonate, CaCO3) is commonly used in the extraction of iron from a blast furnace primarily for two purposes:

A

Limestone (calcium carbonate, CaCO3) is commonly used in the extraction of iron from a blast furnace primarily for two purposes:Fluxing Agent: Limestone is added to the blast furnace as a fluxing agent. In the high-temperature environment of the blast furnace, limestone decomposes to form calcium oxide (CaO) and carbon dioxide (CO2). The calcium oxide reacts with impurities in the iron ore, such as silica (SiO2), to form a slag, which is a molten mixture of calcium silicate (CaSiO3) and other impurities. The slag floats on top of the molten iron and is easily separated, allowing impurities to be removed from the iron.[ \text{CaCO}_3 \rightarrow \text{CaO} + \text{CO}_2 ]Control of Sulfur Content: Limestone also helps control the sulfur content in the blast furnace. When limestone decomposes, some sulfur impurities in the iron ore combine with the calcium oxide to form calcium sulfide (CaS). This calcium sulfide is then removed as part of the slag, helping to reduce the sulfur content in the iron produced.[ \text{CaO} + \text{FeS} \rightarrow \text{CaS} + \text{FeO} ]Overall, the addition of limestone to the blast furnace helps improve the efficiency of the iron extraction process by facilitating the removal of impurities and controlling the sulfur content in the final iron product.

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8
Q

Aromatics and aliphatic compounds can be distinguished using bromine in different reaction conditions:

A

Aromatics and aliphatic compounds can be distinguished using bromine in different reaction conditions:

1.	Bromine Test for Alkenes (Unsaturated Compounds):
•	Aliphatic compounds containing carbon-carbon double bonds (alkenes) readily react with bromine () in an addition reaction. The reddish-brown color of bromine disappears as it adds across the double bond, forming a colorless compound. This reaction is rapid and does not require the presence of light or heat.
•	Aromatics, on the other hand, do not readily react with bromine under normal conditions because the benzene ring is stable and does not undergo addition reactions with bromine.
2.	Bromine Test for Alkanes (Saturated Compounds):
•	In the presence of ultraviolet (UV) light or heat, alkanes (both aliphatic and aromatic) can react with bromine () in a substitution reaction. The color of bromine fades as it substitutes one of the hydrogen atoms in the alkane, forming a bromoalkane.
•	However, alkanes react more slowly with bromine compared to alkenes, and the reaction requires the presence of UV light or heat to proceed. This reaction is not commonly used as a test to distinguish between aromatics and aliphatics due to its slower rate and the need for specific reaction conditions.

In summary, the bromine test for unsaturated compounds (alkenes) is more commonly used to distinguish between aromatics and aliphatics, as alkenes readily react with bromine under normal conditions to form colorless compounds, while aromatics do not undergo addition reactions with bromine.

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9
Q

Sure, here are examples of primary, secondary, and tertiary amines along with their differences:

A
  1. Primary Amine:
    • Example: Ethylamine ()
    • Structure: In ethylamine, the nitrogen atom () is directly bonded to one hydrogen atom () and one ethyl group ().
    • Characteristics: Primary amines have one alkyl or aryl group attached to the nitrogen atom. They can undergo substitution reactions to form secondary and tertiary amines.
    1. Secondary Amine:
      • Example: Dimethylamine ()
      • Structure: In dimethylamine, the nitrogen atom is directly bonded to two methyl groups ().
      • Characteristics: Secondary amines have two alkyl or aryl groups attached to the nitrogen atom. They can undergo substitution reactions to form tertiary amines.
    2. Tertiary Amine:
      • Example: Trimethylamine ()
      • Structure: In trimethylamine, the nitrogen atom is directly bonded to three methyl groups ().
      • Characteristics: Tertiary amines have three alkyl or aryl groups attached to the nitrogen atom. They cannot undergo further substitution reactions at the nitrogen atom due to the absence of hydrogen atoms.

Differences:

•	The main difference between primary, secondary, and tertiary amines lies in the number of alkyl or aryl groups attached to the nitrogen atom.
•	Primary amines have one, secondary amines have two, and tertiary amines have three alkyl or aryl groups attached to the nitrogen atom.
•	This structural difference affects their reactivity in chemical reactions. For example, primary amines can be further substituted to form secondary and tertiary amines, while tertiary amines cannot undergo further substitution reactions at the nitrogen atom.
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10
Q

Sure, here are examples of primary, secondary, and tertiary amines along with their differences:

A
  1. Primary Amine:
    • Example: Ethylamine ()
    • Structure: In ethylamine, the nitrogen atom () is directly bonded to one hydrogen atom () and one ethyl group ().
    • Characteristics: Primary amines have one alkyl or aryl group attached to the nitrogen atom. They can undergo substitution reactions to form secondary and tertiary amines.
    1. Secondary Amine:
      • Example: Dimethylamine ()
      • Structure: In dimethylamine, the nitrogen atom is directly bonded to two methyl groups ().
      • Characteristics: Secondary amines have two alkyl or aryl groups attached to the nitrogen atom. They can undergo substitution reactions to form tertiary amines.
    2. Tertiary Amine:
      • Example: Trimethylamine ()
      • Structure: In trimethylamine, the nitrogen atom is directly bonded to three methyl groups ().
      • Characteristics: Tertiary amines have three alkyl or aryl groups attached to the nitrogen atom. They cannot undergo further substitution reactions at the nitrogen atom due to the absence of hydrogen atoms.

Differences:

•	The main difference between primary, secondary, and tertiary amines lies in the number of alkyl or aryl groups attached to the nitrogen atom.
•	Primary amines have one, secondary amines have two, and tertiary amines have three alkyl or aryl groups attached to the nitrogen atom.
•	This structural difference affects their reactivity in chemical reactions. For example, primary amines can be further substituted to form secondary and tertiary amines, while tertiary amines cannot undergo further substitution reactions at the nitrogen atom.
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11
Q

The relatively high boiling points of alcohols are primarily due to the presence of hydrogen bonding between alcohol molecules.

A

The relatively high boiling points of alcohols are primarily due to the presence of hydrogen bonding between alcohol molecules. Hydrogen bonding occurs when a hydrogen atom attached to a highly electronegative atom (such as oxygen or nitrogen) interacts with another electronegative atom in a neighboring molecule.

In the case of alcohols, the hydrogen atom attached to the oxygen atom in one alcohol molecule can form a hydrogen bond with the lone pair of electrons on the oxygen atom of another alcohol molecule. This intermolecular hydrogen bonding leads to stronger attractive forces between alcohol molecules, requiring more energy to overcome and thus resulting in higher boiling points compared to hydrocarbons of similar molecular weights.

Additionally, the longer the carbon chain in the alcohol molecule, the greater the surface area available for intermolecular interactions, further increasing the strength of the intermolecular forces and contributing to higher boiling points.

In summary, the relatively high boiling points of alcohols compared to hydrocarbons of similar molecular weights are primarily attributed to the presence of hydrogen bonding between alcohol molecules.

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12
Q

When an alkyne reacts with hydrogen iodide (HI), it undergoes an addition reaction known as hydrohalogenation to form an alkyl iodide.

A

When an alkyne reacts with hydrogen iodide (HI), it undergoes an addition reaction known as hydrohalogenation to form an alkyl iodide. The final product depends on the structure of the alkyne.
1. Terminal Alkyne (Acetylene):
• Terminal alkynes react with hydrogen iodide to form vinyl iodides.
• For example, acetylene (CH2) reacts with hydrogen iodide to form vinyl iodide
(CH, = CHI).
2. Internal Alkyne:
• Internal alkynes react with hydrogen iodide to form geminal diiodides (1,2-diiodoalkanes).
• For example, 2-butyne (C4#6) reacts with hydrogen iodide to form 2,2-diiodobutane (CHI2).
The general reaction mechanism involves the addition of hydrogen iodide across the triple bond of the alkyne, resulting in the formation of an alkene intermediate, which subsequently reacts with another molecule of hydrogen iodide to form the final product.
The reaction can be summarized as follows:
Alkyne + HI → Alkyl iodide
It’s important to note that the addition of hydrogen iodide to alkynes follows Markovnikov’s rule, where the iodine atom adds to the carbon atom of the triple bond with the greatest number of hydrogen atoms

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13
Q

n-Heptane

A

n-Heptane is a paraffin hydrocarbon that is particularly prone to causing knocking in internal combustion engines.

n-Heptane is a straight-chain alkane hydrocarbon with seven carbon atoms (C7H16). It is a major component of gasoline and is often used as a reference standard for the octane rating scale. However, despite its importance in gasoline, n-heptane has a relatively low octane rating and is highly prone to causing knocking when used as a fuel in internal combustion engines.

Because of its tendency to cause knocking, n-heptane is typically not used as the sole component of gasoline. Instead, gasoline blends contain various additives and other hydrocarbons with higher octane ratings to improve engine performance and reduce the risk of knocking.

Thank you for bringing up n-heptane as an example of an undesirable paraffin hydrocarbon prone to knocking.​⬤

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14
Q

Steel

A

Chromium and nickel improve quality of steel

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15
Q

Coal gas

A

Coal gas, also known as coal-derived gas, is a gaseous mixture produced by the destructive distillation of coal. The composition of coal gas can vary depending on factors such as the type of coal used, the temperature of the distillation process, and the specific production methods employed. However, typical components of coal gas include:

1.	Hydrogen (H2): Hydrogen is one of the primary components of coal gas and is typically present in significant amounts. It is often the main combustible component and contributes to the heating value of coal gas.
2.	Methane (CH4): Methane, the main component of natural gas, is also present in coal gas. It is a valuable fuel and contributes to the energy content of the gas.
3.	Carbon Monoxide (CO): Carbon monoxide is produced during the incomplete combustion of coal and is a common component of coal gas. It is a toxic gas but can be used as a fuel in certain applications.
4.	Carbon Dioxide (CO2): Carbon dioxide is formed as a byproduct of combustion reactions and is present in coal gas, albeit in smaller quantities compared to carbon monoxide.
5.	Hydrocarbons: Coal gas may contain various hydrocarbons such as ethylene, propylene, and other alkanes and alkenes produced during the distillation process.
6.	Tar and Other Impurities: Coal gas may also contain tar, sulfur compounds, ammonia, and other impurities depending on the source and production process.

It’s important to note that coal gas is not commonly used today due to its high levels of pollutants and the availability of cleaner and more efficient energy sources such as natural gas and electricity. However, coal gas historically played a significant role in providing lighting, heating, and cooking fuel before the widespread adoption of cleaner alternatives.

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16
Q

K L M N

A

2 8 18 32

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17
Q

Coffee stain

A

Solution of borax in water

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18
Q

Acid used to remove rust

A

Tetraoxosulphate (vi)

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19
Q

CaSo4

A

Slightly soluble in water

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20
Q

The IUPAC name for ( \text{LiAlH}_4 ) is Lithium aluminium hydride.

A

The IUPAC name for ( \text{LiAlH}_4 ) is Lithium aluminium hydride.Here’s the breakdown:”Lithium” represents the cation (Li⁺), which is a metal in this compound.”Aluminium” represents the central atom (Al), which is bonded to hydrogen.”Hydride” indicates that hydrogen (H⁻) is present in the compound.So, the compound is named as “Lithium aluminium hydride.”

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21
Q

Tartaric acid

A

Component of baking powder

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22
Q

Calcium oxide heated with carbon

A

Converted to carbide

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23
Q

Cathode rays

A

Certainly, here are some key points about cathode rays:

1.	Discovery: Cathode rays were discovered by Sir William Crookes in 1879. He observed that when a high voltage was applied across electrodes in a vacuum tube, a fluorescent glow appeared on the glass wall near the cathode (negative electrode).
2.	Nature: Cathode rays are streams of electrons emitted from the cathode (negative electrode) in a vacuum tube when a high voltage is applied across the electrodes. They travel in straight lines and can cast shadows, indicating their particle-like nature.
3.	Properties:
•	Cathode rays are negatively charged particles, later identified as electrons.
•	They have a very small mass compared to atoms.
•	They travel at high speeds, typically a significant fraction of the speed of light.
•	They can be deflected by electric and magnetic fields, indicating their charge and the particle nature.
4.	Role in Discoveries:
•	The discovery of cathode rays played a crucial role in the development of atomic theory and the understanding of electricity and magnetism.
•	J.J. Thomson’s experiments with cathode rays led to the identification of electrons as fundamental particles present in atoms, and his discovery of the electron’s charge-to-mass ratio helped lay the groundwork for the development of the atomic model.
5.	Applications:
•	Cathode ray tubes (CRTs) were widely used in old television sets, computer monitors, and oscilloscopes. In CRTs, a beam of electrons is used to produce images on a fluorescent screen.
•	Cathode rays are also used in electron microscopy, where they are focused to produce highly detailed images of microscopic objects.

Overall, the study of cathode rays has significantly contributed to our understanding of the fundamental nature of matter and has led to the development of various technologies with important practical applications.

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24
Q

Negatively Charged: cathode ray

A

Negatively Charged:
• Experiment: Thomson’s Cathode Ray Tube Experiment
• Setup: A cathode ray tube (CRT) is used, consisting of a vacuum tube with electrodes connected to a high voltage source. The cathode (negative electrode) emits cathode rays, which pass through the tube towards the anode (positive electrode).
• Observation: When a magnetic field is applied perpendicular to the path of the cathode rays, they are deflected towards the positively charged plate, indicating that they are negatively charged particles.

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25
Q

Has Mass: cathode ray

A

• Experiment: Thomson’s Measurement of e/m Experiment
• Setup: Using the same cathode ray tube setup as before, Thomson applied both electric and magnetic fields perpendicular to each other and to the direction of the cathode rays.
• Observation: By measuring the extent of deflection caused by the electric and magnetic fields and knowing the strength of the fields, Thomson was able to determine the charge-to-mass ratio (e/m) of the cathode rays. This experiment showed that cathode rays have mass, as they are deflected by both electric and magnetic fields.

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26
Q

Travelling in Straight Lines: cathode ray

A

Travelling in Straight Lines:
• Experiment: Crookes’ Maltese Cross Experiment
• Setup: A cathode ray tube with a Maltese cross-shaped object placed between the cathode and the anode.
• Observation: When the cathode rays pass through the tube, they cast sharp shadows of the Maltese cross on the fluorescent screen placed at the end of the tube. This indicates that the cathode rays travel in straight lines and are not easily deviated from their path.

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27
Q

Quantum numbers

A

The principal quantum number ((n)), azimuthal quantum number ((l)), magnetic quantum number ((m_l)), and spin quantum number ((m_s)) are quantum numbers used to describe the characteristics of an electron in an atom. Here’s a brief explanation of each:Principal Quantum Number ((n)):Represents the energy level or shell of an electron in an atom.Determines the size and energy of an orbital.The value of (n) can be any positive integer (1, 2, 3, …).Azimuthal Quantum Number ((l)):Also known as the orbital angular momentum quantum number.Specifies the shape of an orbital.The value of (l) depends on the value of (n) and ranges from 0 to (n - 1).For (n = 1), (l) can only be 0 (s orbital). For (n = 2), (l) can be 0 or 1 (s or p orbitals), and so on.Magnetic Quantum Number ((m_l)):Describes the orientation of an orbital in space.The value of (m_l) depends on the value of (l) and ranges from (-l) to (l).For example, if (l = 1) (p orbital), (m_l) can be -1, 0, or 1, representing the three possible orientations of the p orbital along the x, y, and z axes.Spin Quantum Number ((m_s)):Describes the intrinsic angular momentum or spin of an electron.An electron can have one of two possible spin states: spin-up ((m_s = +\frac{1}{2})) or spin-down ((m_s = -\frac{1}{2})).The spin quantum number distinguishes between these two states.These quantum numbers are used to describe the quantum mechanical behavior of electrons in atoms and are crucial for understanding the electronic structure and properties of elements. They provide a framework for predicting the arrangement of electrons in atomic orbitals and determining the chemical behavior of atoms.

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28
Q

Photographer’s flash tube

A

Krypton and xenon

29
Q

Oxidation of ammonia in excess

A

NO

30
Q

Hydrogen sulphide can act as

A

Precipitating agent

31
Q

The gasification of coke is used for the manufacture of synthesis gas

A

, commonly referred to as syngas. Syngas is a mixture of carbon monoxide (CO) and hydrogen (H2), along with smaller amounts of carbon dioxide (CO2) and other gases.

Gasification of coke involves reacting coke (which is nearly pure carbon) with a controlled amount of oxygen or steam at high temperatures in a gasifier. This process breaks down the carbon in the coke, releasing gases such as CO and H2. The reaction can be represented by the following equation:

C + H2O → CO + H2

The produced syngas can then be used as a versatile feedstock for various industrial processes, including:

1.	Chemical Synthesis: Syngas can be used as a precursor for the production of a wide range of chemicals, including methanol, ammonia, and synthetic fuels. These chemicals are used in the manufacture of plastics, fertilizers, pharmaceuticals, and other products.
2.	Fuel Production: Syngas can be further processed to produce synthetic fuels such as synthetic natural gas (SNG), hydrogen, and synthetic diesel or gasoline. These fuels can be used for heating, power generation, and transportation, providing alternatives to traditional fossil fuels.
3.	Electricity Generation: Syngas can be combusted in gas turbines or used in fuel cells to generate electricity. This process, known as integrated gasification combined cycle (IGCC), is an efficient and environmentally friendly method of electricity generation that can utilize a variety of feedstocks, including coke.
4.	Carbon Capture and Storage (CCS): The gasification process can be combined with carbon capture and storage technologies to reduce greenhouse gas emissions. CO2 captured from syngas production can be sequestered underground or used in industrial processes such as enhanced oil recovery.

Overall, gasification of coke for the manufacture of syngas is a versatile and efficient process with applications in various industries, providing a valuable pathway for the utilization of carbonaceous feedstocks and the production of clean energy and chemicals.

32
Q

The simplest branched-chain hydrocarbon is

A

propane (C3H8). It consists of a chain of three carbon atoms with each carbon atom bonded to three hydrogen atoms. Propane is a colorless and odorless gas at room temperature and is commonly used as a fuel for heating, cooking, and powering appliances such as grills and stoves.

33
Q

An organic compound that reacts with bromine water to give a colorless solution

A

An organic compound that reacts with bromine water to give a colorless solution is likely to be an unsaturated compound, such as an alkene or alkyne.When bromine water (aqueous solution of bromine) is added to an unsaturated compound, such as an alkene or alkyne, the bromine undergoes addition reactions. The double or triple bond in the unsaturated compound breaks, and bromine atoms add across the carbon-carbon double or triple bond.For example, with an alkene: [ \text{C}_2\text{H}_4 + \text{Br}_2 \rightarrow \text{C}_2\text{H}_4\text{Br}_2 ]In this reaction, the color of bromine water fades as the bromine is consumed in the addition reaction, resulting in a colorless solution.This type of reaction is commonly used to test for the presence of carbon-carbon double or triple bonds in organic compounds. If a compound reacts with bromine water and forms a colorless solution, it indicates the presence of unsaturation in the compound.

34
Q

Dipolar ions

A

Amino acids exist as dipolar ions

35
Q

Lucas reagent, which is a solution of concentrated hydrochloric acid (HCl) and zinc chloride (ZnCl2), is commonly used to test for the presence of

A

alcohol functional groups in organic compounds.

Specifically, Lucas reagent is used to differentiate between primary, secondary, and tertiary alcohols based on the rate of formation of alkyl halides (chlorides) through an SN1 reaction.

•	Primary alcohols: Primary alcohols react slowly with Lucas reagent and may not form a visible precipitate immediately.
•	Secondary alcohols: Secondary alcohols react moderately quickly with Lucas reagent, forming a cloudy or milky solution due to the formation of an alkyl chloride.
•	Tertiary alcohols: Tertiary alcohols react rapidly with Lucas reagent, producing an immediate and distinct cloudy or milky solution due to the rapid formation of alkyl chlorides.

This difference in reactivity is attributed to the stability of the carbocation intermediate formed during the SN1 reaction. Tertiary carbocations are more stable than secondary carbocations, which are in turn more stable than primary carbocations. As a result, tertiary alcohols undergo the SN1 reaction more readily and form alkyl halides more quickly than secondary and primary alcohols when treated with Lucas reagent.

Overall, the Lucas test is a useful qualitative test for distinguishing between primary, secondary, and tertiary alcohols based on their reactivity with Lucas reagent.

36
Q

Molten cryolite ((Na_3AlF_6))

A

Molten cryolite ((Na_3AlF_6)) plays a crucial role in the electrolytic extraction of aluminum from alumina ((Al_2O_3)) in the Hall-Héroult process. The function includes:Lowering the Melting Point: Pure alumina ((Al_2O_3)) has a very high melting point (over 2000°C), making it impractical to use in traditional electrolysis. Molten cryolite serves as a flux, reducing the melting point of the mixture to around 950-1000°C, significantly reducing the energy required for the process.Solvent for Alumina: Cryolite serves as a solvent for alumina, dissolving it and allowing it to conduct electricity. This enables the alumina to dissociate into aluminum ions ((Al^{3+})) and oxygen ions ((O^{2-})) in the molten cryolite.Improving Conductivity: Molten cryolite increases the conductivity of the electrolyte, allowing for efficient transportation of aluminum ions ((Al^{3+})) to the cathode, where they are reduced to form molten aluminum metal.Stabilizing the Electrolyte: Cryolite helps stabilize the electrolyte and prevents it from decomposing at high temperatures, ensuring the continuity and efficiency of the electrolysis process over extended periods.Reducing Environmental Impact: The use of molten cryolite reduces the energy consumption and environmental impact of the aluminum extraction process compared to traditional methods, making it more sustainable and cost-effective.Overall, molten cryolite serves as a vital component in the Hall-Héroult process, enabling the efficient and economical extraction of aluminum from alumina ore.

37
Q

Lead-Acid Battery (Lead Accumulator):

A

Lead-Acid Battery (Lead Accumulator):
• The lead-acid battery, also known as the lead accumulator, is a rechargeable electrochemical cell commonly used in vehicles and backup power systems.
• It consists of a series of lead dioxide (PbO2) positive plates and spongy lead (Pb) negative plates immersed in a sulfuric acid (H2SO4) electrolyte.
• During discharge, lead dioxide undergoes reduction at the positive electrode (cathode), while spongy lead undergoes oxidation at the negative electrode (anode), producing lead sulfate (PbSO4) and releasing electrical energy.
• During charging, the process is reversed, converting lead sulfate back into lead dioxide and spongy lead while absorbing electrical energy.

38
Q

Leclanché Cell:

A

• The Leclanché cell is a primary (non-rechargeable) electrochemical cell commonly used in early portable devices such as flashlights and doorbells.
• It consists of a zinc (Zn) anode, a manganese dioxide (MnO2) cathode, and a porous pot containing a saturated ammonium chloride (NH4Cl) electrolyte.
• During discharge, zinc undergoes oxidation at the anode, releasing electrons and forming zinc ions (), while manganese dioxide undergoes reduction at the cathode, absorbing electrons and forming manganese oxide () and water ().
• The Leclanché cell operates based on the chemical reaction between zinc and manganese dioxide in the presence of ammonium chloride electrolyte.

39
Q

Daniel Cell:

A

• The Daniel cell, invented by John Frederic Daniell, is an early example of a voltaic (galvanic) cell used to generate electrical energy.
• It consists of a copper (Cu) cathode immersed in a solution of copper sulfate () and a zinc (Zn) anode immersed in a solution of zinc sulfate (), separated by a porous barrier or salt bridge.
• During discharge, zinc undergoes oxidation at the anode, releasing electrons and forming zinc ions (), while copper ions () are reduced to copper metal at the cathode, absorbing electrons.
• The Daniel cell operates based on the redox reaction between zinc and copper ions in their respective solutions.

40
Q

Voltaic Cell:

A

• A voltaic cell is any electrochemical cell that converts chemical energy into electrical energy through spontaneous redox reactions.
• It typically consists of two different electrodes (anode and cathode) immersed in an electrolyte solution.
• During discharge, oxidation occurs at the anode, releasing electrons, while reduction occurs at the cathode, absorbing electrons.
• The potential difference between the two electrodes drives the flow of electrons through an external circuit, generating an electric current.

41
Q

Zinc and carbon are used as the anode and cathode, respectively, in the

A

Leclanché cell.

In the Leclanché cell:

•	Anode: Zinc (Zn)
•	Cathode: Carbon (usually in the form of graphite) coated with manganese dioxide (MnO2)

The Leclanché cell is a primary (non-rechargeable) electrochemical cell commonly used in early portable devices such as flashlights and doorbells.

42
Q

The overall reaction occurring during the electrolysis of copper sulfate can be represented as follows:

A

At the anode (positive electrode):
2H,0 → 02 + 4Ht + 4€
CuSO, → Cut + S03-
Cut + 26 → Cu
At the cathode (negative electrode):
Cu?t + 26 → Cu
The platinum electrodes serve as inert conductors, meaning they do not participate in the chemical reactions themselves but simply facilitate the transfer of electrons between the electrolyte and the external circuit.
At the anode, water molecules are oxidized to oxygen gas and protons (H-). Additionally, copper ions (Cuz+) from the copper sulfate solution are also oxidized to copper metal (Cu). This process is known as the anodic reaction.
At the cathode, copper ions (Cu?+) from the copper sulfate solution are reduced to copper metal (Cu).
This process is known as the cathodic reaction.

43
Q

Nuclear fission

A

is a nuclear reaction in which the nucleus of an atom splits into two or more smaller nuclei, along with the release of a large amount of energy. This process typically occurs in heavy elements such as uranium-235 () or plutonium-239 ().

The process of nuclear fission can be initiated by bombarding a heavy nucleus with a neutron. When the nucleus absorbs the neutron, it becomes unstable and splits into two or more smaller nuclei, known as fission fragments. Additionally, several neutrons are typically released during the fission process.

The key components of nuclear fission are:

1.	Initiation: A heavy nucleus, such as uranium-235, absorbs a neutron, becoming unstable.
2.	Splitting: The unstable nucleus undergoes fission, splitting into two or more smaller nuclei, known as fission fragments. This process releases a large amount of energy in the form of kinetic energy and gamma radiation.
3.	Neutron Release: Several neutrons are typically released during the fission process. These neutrons can go on to initiate further fission reactions in nearby nuclei, leading to a chain reaction.

Nuclear fission is the process that powers nuclear reactors, which are used for electricity generation, propulsion of nuclear submarines, and various other applications. It is also the basis for nuclear weapons, where controlled or uncontrolled fission reactions release enormous amounts of energy in a short period of time.

44
Q

Rutherford

A

Planetary model

45
Q

Copper sulphide

A

Insoluble in dilute copper sulphide

46
Q

Ammonia

A

Ammonium salt heated with base

47
Q

Conversion of silver ion to silver metal

A

Photochemical reaction

48
Q

Sulfide ores are one of the most common types of ores concentrated by flotation. Sulfide minerals typically contain metal ions bonded to sulfur ions and can be concentrated using froth flotation due to their hydrophobic nature. Some of the sulfide ores commonly concentrated by flotation include:

A
  1. Copper Sulfide Ores: Copper sulfide ores, such as chalcopyrite (CuFeS2), bornite (Cu5FeS4), and chalcocite (Cu2S), are frequently concentrated by flotation. The copper minerals are usually floated first, followed by the flotation of other sulfide minerals or gangue minerals.
    1. Lead-Zinc Sulfide Ores: Ores containing lead and zinc sulfide minerals, such as galena (PbS) and sphalerite (ZnS), are often concentrated by flotation. The separation of lead and zinc minerals is achieved through selective flotation, where collectors are used to preferentially float one mineral over the other.
    2. Nickel Sulfide Ores: Nickel sulfide ores, including pentlandite ((Ni,Fe)9S8) and nickeliferous pyrrhotite ((Ni,Fe)1-xS), can be concentrated by flotation. The flotation process allows for the separation of nickel minerals from gangue minerals based on their different surface properties.
    3. Iron Sulfide Ores: Iron sulfide ores, such as pyrite (FeS2) and pyrrhotite (Fe1-xS), can also be concentrated by flotation. In some cases, these sulfide minerals are removed during flotation to improve the iron content of the concentrate.
    4. Molybdenum Sulfide Ores: Molybdenum sulfide ores, such as molybdenite (MoS2), are concentrated by flotation to produce a molybdenum concentrate. The separation of molybdenum minerals from gangue minerals is achieved through selective flotation.
    5. Silver Sulfide Ores: Ores containing silver sulfide minerals, such as argentite (Ag2S), can be concentrated by flotation to produce a silver concentrate.
    6. Gold-Sulfide Ores: Some gold ores containing sulfide minerals, such as pyrite and arsenopyrite, can be concentrated by flotation. This process is commonly used in gold ore processing to recover gold-bearing sulfide minerals.

Overall, sulfide ores are amenable to concentration by flotation due to the hydrophobic nature of sulfide minerals, which allows them to be selectively floated from gangue minerals in the ore.

49
Q

The term “metalloids” refers to elements that have properties intermediate between those of metals and nonmetals.

A

The term “metalloids” refers to elements that have properties intermediate between those of metals and nonmetals. These elements exhibit characteristics of both metals and nonmetals, making their classification somewhat ambiguous. The most commonly recognized metalloids are boron (B), silicon (Si), germanium (Ge), arsenic (As), antimony (Sb), and tellurium (Te).

Metalloids typically possess some metallic properties, such as electrical conductivity, but also exhibit nonmetallic properties, such as brittleness and semiconductor behavior. Their properties depend on various factors such as their position in the periodic table, atomic structure, and bonding characteristics.

In some cases, metalloids are used in semiconductor technology, as they can be doped to control the electrical conductivity of materials. For example, silicon is a key component of semiconductors used in electronic devices.

50
Q

The most abundant element in the Earth’s crust by mass is

A

oxygen. Oxygen makes up approximately 46.6% of the Earth’s crust by mass. This is largely due to the prevalence of oxygen in minerals such as silicates, oxides, and carbonates, which are the primary constituents of the Earth’s crust. Silicon is the second most abundant element in the Earth’s crust, followed by aluminum, iron, calcium, sodium, potassium, and magnesium.

51
Q

Arrhenius law

A

, formulated by the Swedish chemist Svante Arrhenius in 1889, describes the temperature dependence of chemical reaction rates. The law states that the rate constant ((k)) of a chemical reaction increases exponentially with an increase in temperature ((T)) according to the equation:[ k = A \times e^{-\frac{E_a}{RT}} ]Where:( k ) is the rate constant,( A ) is the pre-exponential factor or frequency factor, representing the frequency of collisions between reactant molecules,( E_a ) is the activation energy, the minimum energy required for a reaction to occur,( R ) is the universal gas constant (8.314 J/mol·K),( T ) is the absolute temperature in Kelvin, and( e ) is the base of the natural logarithm.Key points of Arrhenius law include:Temperature Dependence: The rate constant of a reaction increases exponentially with increasing temperature. This reflects the greater fraction of reactant molecules possessing sufficient energy to overcome the activation energy barrier and undergo reaction.Activation Energy: The activation energy is a measure of the energy barrier that reactant molecules must overcome to form products. Higher activation energies result in slower reaction rates, as fewer reactant molecules possess the necessary energy to overcome the barrier.Pre-exponential Factor: The pre-exponential factor (( A )) accounts for the frequency of successful collisions between reactant molecules. It represents the rate at which reactant molecules approach each other in the correct orientation for reaction to occur.Exponential Relationship: The exponential relationship between temperature and reaction rate emphasizes the sensitivity of reaction rates to temperature changes. Even small increases in temperature can lead to significant increases in reaction rates.Arrhenius law has important implications in various fields of chemistry and is widely used to understand and predict the behavior of chemical reactions under different temperature conditions. It forms the basis for understanding the temperature dependence of reaction kinetics and plays a crucial role in areas such as chemical kinetics, reaction engineering, and materials science.

52
Q

When pure aluminum is heated to red-hot

A

When pure aluminum is heated to red-hot temperatures in the presence of nitrogen, it can react with nitrogen to form aluminum nitride (AIN).
This reaction typically occurs at high temperatures above 1000°C (1832°F) when aluminum is in contact with nitrogen gas (N2). The reaction between aluminum and nitrogen can be represented by the following equation:
2A1 + 3N2 → 2AIN
Aluminum nitride is a ceramic compound with a high melting point and excellent thermal conductivity. It is commonly used in applications such as semiconductor manufacturing, thermal management, and as a component in cutting tools and abrasives.

53
Q

The air around smelting industries can contain various pollutants, depending on the specific smelting process and the materials being processed. Some of the common pollutants found in the air around smelting industries include:

A

The air around smelting industries can contain various pollutants, depending on the specific smelting process and the materials being processed. Some of the common pollutants found in the air around smelting industries include:

1.	Particulate Matter (PM): Smelting operations can generate dust and particulate matter, which may contain metal oxides, sulfides, and other contaminants. These particles can be released into the air during ore crushing, grinding, and handling processes.
2.	Sulfur Dioxide (SO₂): Smelting of sulfide ores, such as those containing copper, lead, and zinc, can release sulfur dioxide gas into the atmosphere. Sulfur dioxide is a harmful air pollutant that can cause respiratory problems and contribute to the formation of acid rain.
3.	Nitrogen Oxides (NOₓ): High-temperature smelting processes can produce nitrogen oxides, such as nitrogen dioxide (NO₂) and nitric oxide (NO). These compounds are formed through the combustion of nitrogen in the air and can contribute to air pollution and smog formation.
4.	Heavy Metals: Smelting activities can release heavy metals such as lead, mercury, arsenic, and cadmium into the air. These metals can pose serious health risks to humans and the environment, especially if they are inhaled or deposited onto soil and water.
5.	Volatile Organic Compounds (VOCs): Some smelting processes may involve the use of organic solvents, fuels, or other chemicals that can release volatile organic compounds into the air. VOCs can contribute to air pollution and may have adverse health effects.
6.	Carbon Monoxide (CO): Incomplete combustion of carbon-containing materials, such as coal or coke used in smelting operations, can produce carbon monoxide gas. Carbon monoxide is a toxic gas that can cause poisoning and adverse health effects when inhaled.
7.	Particulate Metals: Fine particles of metals, such as aluminum, copper, and zinc, may be emitted into the air as aerosols during smelting processes. These particulate metals can contribute to air pollution and may have adverse effects on human health and the environment.

Overall, the air around smelting industries may contain a complex mixture of pollutants that can vary depending on the specific operations and the control measures in place to mitigate emissions. Efforts to reduce emissions from smelting industries are essential for protecting human health and the environment.

54
Q

Cyclohexane has _____ hydrogen atoms less than benzene

A

2

55
Q

If an aluminum spoon is used to stir a solution of iron(III) trioxonitrate(V), also known as iron(III) nitrate, several reactions may occur:

A

Redox Reaction: Aluminum (Al) is a more reactive metal than iron (Fe), so it can displace iron from its compounds. In this case, aluminum may react with iron(III) ions in the solution according to the following reaction:[ 2Al(s) + 3Fe(NO_3)_3(aq) \rightarrow 2Al(NO_3)_3(aq) + 3Fe(s) ]This reaction results in the formation of aluminum nitrate ((Al(NO_3)_3)) in solution and the deposition of iron metal ((Fe)).Release of Hydrogen Gas: In addition to displacing iron from its compound, aluminum may also react with water ((H_2O)) present in the solution to produce hydrogen gas ((H_2)):[ 2Al(s) + 6H_2O(l) \rightarrow 2Al(OH)_3(aq) + 3H_2(g) ]This reaction produces aluminum hydroxide ((Al(OH)_3)), which is a white precipitate, and hydrogen gas bubbles.Corrosion of Aluminum: Aluminum is also susceptible to corrosion in the presence of oxygen and moisture. The acidic nature of the iron(III) nitrate solution may accelerate the corrosion process, leading to the formation of aluminum oxide ((Al_2O_3)) and the release of hydrogen gas:[ 2Al(s) + 3O_2(g) \rightarrow 2Al_2O_3(s) ]Overall, using an aluminum spoon to stir a solution of iron(III) trioxonitrate(V) may result in the displacement of iron, the release of hydrogen gas, and the corrosion of the aluminum spoon. It is generally not recommended to use reactive metals such as aluminum with solutions containing other metal ions, as it can lead to unwanted reactions and damage to the equipment.

56
Q

When excess sulfur ((S_8)) is passed into a solution of sodium hydroxide ((NaOH)) for a long time, several reactions may occur

A

When excess sulfur ((S_8)) is passed into a solution of sodium hydroxide ((NaOH)) for a long time, several reactions may occur, leading to the formation of thiosulfate and other sulfur-containing compounds. The reaction proceeds as follows:Formation of Sodium Thiosulfate ((Na_2S_2O_3)): [ 4NaOH + 2S_8 \rightarrow Na_2S_2O_3 + 4H_2O ]In this reaction, the sulfur reacts with sodium hydroxide to form sodium thiosulfate ((Na_2S_2O_3)), a compound commonly used in photographic fixing solutions.Formation of Sodium Polysulfides ((Na_2S_x)): [ NaOH + S_8 \rightarrow Na_2S_x + H_2O ]Excess sulfur may also react with sodium hydroxide to form sodium polysulfides ((Na_2S_x)), which are compounds containing multiple sulfur atoms.Hydrolysis of Sodium Polysulfides: [ Na_2S_x + H_2O \rightarrow NaHSO_3 + NaOH ]The sodium polysulfides formed in the previous step can undergo hydrolysis in the presence of water to produce sodium hydrogen sulfite ((NaHSO_3)) and sodium hydroxide.Overall, the reaction of excess sulfur with sodium hydroxide results in the formation of various sulfur-containing compounds, including sodium thiosulfate and sodium polysulfides. These reactions may be used in various industrial processes or chemical applications where sulfur compounds are needed.

57
Q

Bleaching by reduction and oxidation are two different chemical processes used to remove color from substances.

A

Here are the differences between the two processes along with examples:Bleaching by Reduction:Process: Bleaching by reduction involves the addition of reducing agents to a colored substance, which donate electrons to the chromophore groups, thereby breaking the double bonds and reducing the substance’s ability to absorb visible light.Mechanism: The reducing agent reduces the chromophore groups in the colored substance, converting them into colorless compounds.Examples:Hair Bleaching: Hydrogen peroxide ((H_2O_2)) is commonly used to bleach hair. It acts as a reducing agent, breaking down the melanin pigment in the hair shaft, thereby lightening the hair color.Textile Bleaching: Sodium dithionite ((Na_2S_2O_4)), also known as sodium hydrosulfite, is used in textile industries to bleach fabrics and remove color.Bleaching by Oxidation:Process: Bleaching by oxidation involves the addition of oxidizing agents to a colored substance, which accept electrons from the chromophore groups, thereby breaking the double bonds and reducing the substance’s ability to absorb visible light.Mechanism: The oxidizing agent oxidizes the chromophore groups in the colored substance, converting them into colorless compounds.Examples:Household Bleaching: Household bleach, which contains sodium hypochlorite ((NaClO)), is used to remove stains from clothing and disinfect surfaces. The hypochlorite ion ((ClO^-)) acts as an oxidizing agent, oxidizing the colored compounds into colorless forms.Paper Bleaching: Chlorine dioxide ((ClO_2)) is used in the paper industry to bleach wood pulp and remove lignin, which contributes to the yellow color of paper.In summary, bleaching by reduction involves the addition of reducing agents to remove color by breaking down chromophore groups, while bleaching by oxidation involves the addition of oxidizing agents to remove color by oxidizing chromophore groups. Both processes are widely used in various industries, including textile, hair care, and paper manufacturing, to achieve desired color changes or whiteness.

58
Q

Transition metals have variable oxidation states due to their unique electron configurations and the presence of incompletely filled d orbitals in their outer electron shells. Here are the key reasons why transition metals exhibit variable oxidation states:

A
  1. Incompletely Filled d Orbitals: Transition metals have electrons in their d orbitals, which can participate in bonding. The d orbitals have similar energies, allowing electrons to move between them relatively easily. This flexibility allows transition metals to form multiple oxidation states by either losing or gaining electrons from their d orbitals.
    1. Electronic Configuration: The electronic configuration of transition metals often involves the filling of the (n-1)d orbitals before the outer ns orbital. For example, in the case of chromium (Cr), the electron configuration is [Ar] 3d^5 4s^1 instead of the expected [Ar] 3d^4 4s^2. This arrangement allows for different oxidation states depending on whether electrons are lost from the ns orbital or the (n-1)d orbitals.
    2. Ability to Lose or Gain Electrons: Transition metals have the ability to lose electrons from their outer ns orbital or gain electrons into their d orbitals to achieve a stable electron configuration. Since the d orbitals are relatively close in energy, it is energetically feasible for transition metals to adopt multiple oxidation states by redistributing their electrons among these orbitals.
    3. Formation of Complex Ions: Transition metals often form complex ions with ligands (molecules or ions that donate electron pairs to the metal ion). These ligands can influence the oxidation state of the central metal ion by either stabilizing certain oxidation states or facilitating electron transfer reactions.
    4. Coordination Chemistry: In coordination compounds, transition metals can adopt different oxidation states depending on the nature of the ligands and the geometry of the complex. The ligands can exert varying degrees of electron-donating or -withdrawing effects, influencing the oxidation state of the metal ion.

Overall, the combination of the electronic configuration of transition metals, the presence of incompletely filled d orbitals, and their ability to form complex ions and coordination compounds allows them to exhibit variable oxidation states, making them versatile and important in a wide range of chemical reactions and applications.

59
Q

Aluminium hydroxide

A

Mordant for dye

60
Q

Alkaline pyrogallol absorbs

A

Oxygen

61
Q

When steam (water vapor) is passed over red-hot carbon, several reactions can occur, depending on the conditions and the nature of the carbon.

A

When steam (water vapor) is passed over red-hot carbon, several reactions can occur, depending on the conditions and the nature of the carbon. The primary reaction involves the reduction of steam to produce hydrogen gas ((H_2)) and carbon monoxide ((CO)), known as the water-gas shift reaction. The reaction can be represented as follows:[ H_2O(g) + C(s) \rightarrow H_2(g) + CO(g) ]This reaction is endothermic and typically occurs at high temperatures, such as those provided by red-hot carbon. The carbon acts as a reducing agent, providing the necessary electrons to reduce water vapor into hydrogen and carbon monoxide. The produced hydrogen and carbon monoxide are important industrial gases used in various processes, including the production of synthetic fuels, ammonia synthesis, and methanol production.Additionally, if the temperature is high enough, carbon dioxide ((CO_2)) may also react with the carbon to form carbon monoxide according to the following reaction:[ CO_2(g) + C(s) \rightarrow 2CO(g) ]This reaction is known as the Boudouard reaction or carbon gasification and is favored at higher temperatures.Overall, passing steam over red-hot carbon can result in the production of hydrogen gas and carbon monoxide, which are valuable industrial feedstocks for numerous chemical processes.

62
Q

The shape of each orbital is determined by its quantum numbers and is described using mathematical functions called wavefunctions or orbitals. Here are the shapes of the most common types of atomic orbitals:

A
  1. s Orbital:
    • Shape: Spherical
    • Probability Density: Maximum at the nucleus and decreases radially outward
    • Examples: 1s, 2s, 3s, …
    1. p Orbital:
      • Shape: Dumbbell-shaped with two lobes oriented along the x, y, or z axes
      • Probability Density: Maximum in the lobes and zero at the nucleus
      • Examples: 2p, 3p, 4p, …
    2. d Orbital:
      • Shape: Complex shapes with multiple lobes and nodal planes
      • Probability Density: Varies depending on the specific d orbital (e.g., some have four lobes, some have a cloverleaf shape)
      • Examples: 3d, 4d, 5d, …
    3. f Orbital:
      • Shape: Even more complex than d orbitals, with multiple lobes and nodal surfaces
      • Probability Density: Varies significantly depending on the specific f orbital
      • Examples: 4f, 5f, 6f, …

Each orbital also has additional quantum numbers that describe its orientation in space and its energy level within an atom. These quantum numbers include the principal quantum number (n), the azimuthal quantum number (l), the magnetic quantum number (m_l), and the spin quantum number (m_s). Together, these quantum numbers fully describe the size, shape, and orientation of an orbital within an atom.

63
Q

The most common reagent used to confirm the presence of a triple bond (alkyne) is potassium permanganate ((KMnO_4)) solution.

A

Alkynes readily react with potassium permanganate in alkaline conditions (sodium hydroxide, (NaOH)) to form a diol (glycol).The reaction proceeds as follows:[ R-C \equiv C-R + 2KMnO_4 + 3NaOH \rightarrow 2MnO_2 + 2KOH + 2R-C(OH)_2 ]In this reaction, the purple color of the potassium permanganate solution is decolorized as it is reduced to form brown manganese dioxide ((MnO_2)). Additionally, the formation of a diol ((R-C(OH)_2)) confirms the presence of the alkyne functional group.This reaction is often used as a qualitative test for the presence of triple bonds in organic compounds. If a purple solution of potassium permanganate turns brown upon addition to a compound, it indicates the presence of a triple bond.

64
Q

So2

A

Can act as both reducing and oxidising agent

65
Q

Vulcanization

A

Involves removal of double bond

66
Q

Calcium

A

Calcium (Ca) is another metal that liberates hydrogen from cold water with bubbles. When calcium reacts with cold water, it produces hydrogen gas along with calcium hydroxide. The reaction can be represented as follows:

Thank you for pointing out calcium as another example of a metal that reacts with water to liberate hydrogen gas.

67
Q

Chlorine has turns damp starh iodide. Paper

A

Dark blue

68
Q

Structural component that makesxdetergebt dissolve more quickly than soap

A

So3 -NA+