Gases and Solutions Flashcards

1
Q

Kinetic Theory of Gases

A
  1. Gases are composed of particles in rapid, continuous, random motion.
  2. Attraction and repulsion between particles in gases is negligible.
  3. Particles in a gas are widely spaced – the total volume of all the particles is negligible compared to the volume the gas occupies.
  4. Particles in a gas have kinetic energy, given by EK = ½ mv2.
  5. The average EK of all particles in a gas is proportional to its temperature and is the same for all gases at the same temperature.
  6. Particle collisions are elastic – as particles collide, they do not lose speed or energy.
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2
Q

Behaviour of Gases

A
  • Take the shape of their container: constant random motion with negligible forces of attraction, results in gas particles spreading out to occupy the entire volume of the container.
  • Have a very low density: large empty spaces between gas particles, total volume of gas particles is negligible.
  • Exert a pressure: constant random motion results in collisions with container walls – pressure increases with the frequency & force of these collisions.
  • Can be compressed: large empty spaces between gas particles, when compressed, the amount of space between the gas particles decreases (particle size doesn’t change)
  • Readily diffuse through other gases: because gas particles have rapid, random motion and a lot of empty space between them, so they quickly spread and mix.
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3
Q

Temperature

A
  • A measure of average kinetic energy of particles within a substance.
  • Heavier gases have lower speeds than lighter gases.
  • As T (Temperature) increases, EK (Kinetic Energy)increases.
  • At any temperature, gas particles will have a range of speeds.
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4
Q

Temperature Units

A
  • Absolute zero: the theoretical lowest temperature possible (0 K = -273.15 ºC)
  • Kelvin vs ºC
  • 0 K = -273.15°C
  • 10 K = -263.15°C
  • To convert from ºC to K do the following:
  • T(K) = TºC + 273.15
  • To convert from K to ºC do the following:
  • T(ºC) = T(K) – 273.15
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5
Q

Pressure

A
  • Determined by the frequency and force of collisions of the gas particles and the container walls.
  • SI unit pascal (Pa)
  • Standard Pressure = 100 kPa
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6
Q

Gas Laws

A
  • The relationships between T, P & V of gases is described by different laws
  • Boyle’s Law (P, V)
  • Charles’ Law (T, V)
  • Combined Gas law (P, V & T)
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7
Q

Boyle’s Law

A
  • “At constant temperature, the volume of a given mass of gas is inversely proportional to the pressure”.
  • Increasing the volume of a container results in a decrease in the frequency of collisions.
  • More space = less chance of a particle colliding with the container walls.
  • Inversely proportional relationship:
  • Double the volume, halve the pressure!
  • Halve the volume, double the pressure!
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8
Q

Charles’ law

A
  • “At constant pressure, the volume of a fixed quantity of gas is proportional to its absolute temperature”
  • Increasing temperature of the gas increases the average EK and the average velocity of the particles.
  • The gas particles collide with the container walls more frequently and with a greater force.
  • This results in an increase in pressure.
  • For the pressure inside a container to remain constant, the volume of the gas will increase.
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9
Q

Ideal Gas vs Real Gas

A

Real Gas:
* particles in a real gas do occupy volume
* forces of attraction do exist between particles of a real gas

Ideal Gas:
* particle in an ideal gas have negligible volume
* forces of attraction are negligible between particles of an ideal gas

These differences only become important in extreme conditions – at very low temperatures:
1. Theoretically an ideal gas at 0 K would occupy zero volume, but a real gas will never have zero volume because its particles occupy space.
2. If a real gas is compressed or cooled, it will condense to form a liquid due to the intermolecular forces that exist between the particles. However, an ideal gas will never condense because these attractive forces are negligible.

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10
Q

Volume of Gas

A

volume of a gas depends on:
- pressure
- temperature
- amount of gas particles present (moles)

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11
Q

Molar Volume of gases (STP)

A
  • Avogadro’s hypothesis: equal volumes of gases at the same temperature and pressure contain equal numbers of particles
  • the volume of 1 mol of all gases, at the same temperature & pressure is identical
  • At STP (standard temperature and pressure)
  • Temperature: 273.15 K or 0 ºC
  • Pressure: 100.0 kPa
  • n=V/22.71
  • n = number of moles
  • V = volume in litres (L)
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12
Q

Ideal Gas Law

A
  • We need at least one of the conditions of P, T or V and quantity of gas remain constant.
  • In reality, all conditions vary
  • Boyle’s law, Charles’ law and Avogadro’s hypothesis combine to give the Ideal Gas law which includes all conditions as variables.
  • PV=nRT
  • P = pressure in kPa
  • V = volume in L
  • n = number of moles of gas
  • R = universal gas constant 8.314 J K-1 mol-1
  • T = temperature in K
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13
Q

Solutions

A
  • solute: the substance that ‘is dissolved’
  • solvent: the substance that ‘does the dissolving’
  • solution: a homogenous mixture (uniform composition) made up of two or more substances
  • solubility: the ability for a given substance, the solute, to dissolve in a solvent.
  • qualitative: soluble, insoluble, slightly soluble
  • quantitative: mass that can dissolve in 100g of water
  • soluble: able to dissolve
  • insoluble: unable to dissolve
  • solubility is better thought of as a range from infinitely soluble (ethanol in water) to poorly soluble (silver chloride in water)
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14
Q

Water - the Universal Solvent

A
  • Water is often referred to as the universal solvent, (despite the fact it DOES NOT dissolve many compounds).
  • It is such a good solvent due to its polarity.
  • A POLAR molecule has a slight +ve charge at one end and a slight –ve charge at the other end (or DIPOLE).
  • This charge is not as big as the charge on an ion, but none-the-less creates an electrostatic attraction and repulsions with neighbouring molecules.
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15
Q

Solutes

A
  • The solute in a solution is the part in small amounts which dissolves in the solvent.
  • Substances that readily dissolve in water are called HYDROPHILLIC (water loving).
  • Substances that do not dissolve in water are called HYDROPHOBIC (water hating).
  • Solutes can be either:
  • Ionic (metal and non-metal)
  • Polar (molecules containing –OH, C=O, or –NH groups)
  • Non-Polar – but these don’t dissolve in water (long C chains)
  • Substances may dissolve in water will either be polar (like water) or charged (like Ionic substances)
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16
Q

Solubility and Polarity

A
  • Polar substances dissolve in polar solvents but NOT in non-polar substances.
  • Non-Polar substances dissolve in non-polar solvents but NOT in polar solvents.
17
Q

Factors Affecting Solubility

A
  • Very Highly Polar: Ionic Compounds
  • Polar: -OH, C=O or -NH groups in their molecules
  • Non-Polar: Mostly made of carbon and hydrogen
  • Has Both Polar and Non-Polar Properties: Contain -OH groups and carbon and hydrogen atoms
18
Q

Solutes in Water

A
  • Ionic Compounds, such as salts, will be ionic solutes.
  • Other polar molecules, such as ethanol, will be polar solutes.
  • Water will form either ion-dipole bonds, dipole-dipole bonds or hydrogen bonds with these solutes.
  • It is the great number of these interactions that cause these substances to break apart and dissolve.
19
Q

Ionic Solutes in Water

A
  • When NaCl dissolves in water, ion-dipole bonds are formed.
20
Q

Organic Solutes in Water

A
  • Most organic molecules are non-polar and hydrophobic.
  • Molecules containing a large proportion of –OH, C=O and –NH groups may dissolve in water.
21
Q

Ethanol

A
  • Ethanol dissolves in water because of its polar –OH end group.
  • Ethanol also dissolves in organic solvents because it has a non-polar –CH3 end.
22
Q

Solubility

A
  • A solute DISSOLVES when:
  • The energy of the bonds it forms with water is LOWER than the energy of the bonds between the ions/molecules of solute.
  • This energy difference explains why some ionic substances dissolve in water and others don’t.
  • Solubility depends on several factors:
  • Strength of Ionic Bonding
  • Which depends on arrangement of ions in the lattice, size of ions and charges on ions.
  • Strength of Ion-Dipole attraction
  • Which depends on sizes of ions, charges on ions, geometry of ions (if polyatomic).
  • The more energy released by bonds being formed compared with energy needed to separate particles, the more soluble the salt.
23
Q

Saturation

A
  • When a solute is added to a solvent, it will start to dissolve.
  • UNSATURATED SOLUTION – is still capable of dissolving more solute.
  • Once the solution contains the maximum amount of solute the solution is said to be SATURATED, at which stage the rate of dissolving is equal to the rate of re-crystallisation.
  • The solution is said to be SUPERSATURATED if it contains more than the maximum allowable amount of dissolved solute for that temperature. This is usually achieved by dissolving the solute in a hot solvent then allowing it to cool.
  • Above a supersaturated solution of sodium acetate is “seeded” with a crystal to initiate crystallisation. Crystallisation continues until the solution is saturated (no longer supersaturated).
24
Q

Temperature

A
  • Solids Dissolve in Liquids:
  • Temperature: Increase
  • Solubility: Increase
  • Gases in Liquids
  • Temperature: Increase
  • Solubility: Decrease
25
Q

Types of Solutions

A
  • SOLID in SOLID: alloys, silver coins, stainless steel
  • SOLID in LIQUID: sugar in water, salt in water
  • LIQUID in LIQUID: alcohol in water, perfumes
  • GAS in LIQUID: soda drinks, hydrochloric acid
  • GAS in GAS: air
26
Q

Electrolytes

A

When dissolved in water, particles in a:
* strong electrolyte: exist entirely as ions – High Conductivity
* 100% dissociation/ionisation
* weak electrolyte: exist mostly as molecules but partly as ions – Low Conductivity
* significantly less than 100% dissociation/ionisation
* non-electrolyte: exist entirely as molecules & do not produce ions – No Conductivity

27
Q

Dissociation and Ionisation

A
  • dissociation: ions present in an ionic solid are released into solution
  • ionisation: the formation of ions from a molecular substance as it dissolves in water
  • single arrow means reaction goes to completion (100%)
  • double arrow means reaction does not go to completion (partial ionisation)
28
Q

Strong Electrolytes

A
  • Ionic Solids
  • Strong Acids: HCl, HNO3, H2SO4
29
Q

Weak Electrolytes

A
  • Weak Acids: CH3COOH, H3PO4, H2CO3
  • Weak Bases: NH3
30
Q

Chemical Equations

A
  • reactants -> products
  • ‘Law of Conservation of Mass’
  • total mass of reactants = total mass of products
  • this is why equations must be balanced
  • state symbols (s), (l), (g), (aq) must be included
  • double arrows (⇌) indicate a reaction is reversible
31
Q

Common Chemical Reactions

A
  • ACID REACTIONS:
  • ACID + BASE  SALT + WATER
  • ACID + REACTIVE METAL  SALT + HYDROGEN GAS
  • ACID + METAL CARBONATE  SALT + WATER + CARBON DIOXIDE
32
Q

Types of Chemical Equations

A

Molecular equations:
* substances, especially solutions, are represented using full formulas
Net Ionic Equations:
* strong electrolytes are represented as separate ions
* spectator ions are not included
lead nitrate solution added to potassium iodide solution:
* Molecular Equation: Pb(NO3)2(aq) + 2KI(aq) -> PbI2(s) + 2KNO3(aq)
* Net Ionic Equation: Pb2+(aq) + 2I-(aq) -> PbI2(s)