Organic chemistry Flashcards

1
Q

What are hydrocarbons?

A

Compounds that consist of carbon and hydrogen only

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2
Q

What is crude oil?

A

(dark, viscous liquid)

-A complicated mixture of many hydrocarbon molecules of different sizes and shapes

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3
Q

Why/ how is crude oil separated?

A
  • In its raw state, crude oil is virtually useless
  • But it can be refined to extract useful components
  • Refined using the process fractional distillation
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4
Q

State the principles of fractional distillation and how it works?

A
  • The crude oil is vaporised and passed into the bottom of a long column
  • That is hot at the bottom and cool at the top
  • The heavier a compound (the more carbons it has), the higher its boiling point
  • That means that the heavier compounds leave the column first towards the bottom, where the temperature is the highest
  • The really light compounds leave the column towards the top where the temperature is lower
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5
Q

How does the chain length of a hydrocarbon affect it’s boiling point?

A
  • Heavier compounds
  • With longer chains
  • Make larger molecules
  • Have greater intermolecular forces of attraction
  • Require more energy to overcome
  • Have higher boiling points
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6
Q

How does the chain length of a hydrocarbon affect it’s viscosity?

A
  • Heavier compounds
  • With longer chains
  • Are more viscous
  • As longer/ heavier chains are thicker in their liquid form
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7
Q

What is meant by the term “volatility”? How does the chain length of a hydrocarbon affect it’s volatility?

A

“The volatility of a compound is its tendency to evaporate at a given temperature”

  • Heavier compounds
  • With longer chains
  • Are less volatile
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8
Q

How does the chain length of a hydrocarbon affect it’s ability to ignite?

A

Heavier compounds, with longer chains, do not ignite easily

Lighter more shorter chains, ignite more easily

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9
Q

What is catalytic cracking?

A

A second refinement process, that “cracks”/ passes the longer chain molecules from fractional distillation, over a heated catalyst that breaks them into even smaller chained alkanes/ alkenes

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10
Q

What is the molecular formula of a compound?

A

The formula that shows the actual no. of atoms in each element in one molecule of that compound

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11
Q

What is a (displayed/full) structural formula?

A

The formula that specifies/ shows how the atoms are arranged, including all the covalent bonds

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12
Q

What is a (condensed) structural formula?

A

The formula that specifies/ shows how the atoms are arranged, in a compact way (without showing the covalent bonds)

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13
Q

What is meant by the term “structural isomerism”?

A

Structural isomerism arises when it is possible to sequence the atoms in a molecular formula in more than 1 way

  • have the SAME MOLECULAR formula
  • but DIFFERENT STRUCTURAL formula
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14
Q

What is complete combustion?

A

When you burn a hydrocarbon [reacts with oxygen] “properly”, with enough/ excess oxygen and you form carbon dioxide and water, with a release of energy

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15
Q

How would you balance an equation showing COMPLETE combustion?

A
  • The number of molecules of carbon dioxide formed will be given by the number of carbon atoms in the hydrocarbon
  • The number of molecules of water formed will be half of the number of hydrogen atoms in the hydrocarbon
  • All that remains is to balance the oxygen atoms
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16
Q

What is incomplete combustion?

A

When you burn a hydrocarbon [react with oxygen] with an insufficient supply of oxygen, producing carbon monoxide IN ADDITION TO carbon dioxide and water, with a release of energy

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17
Q

What is meant by the term “homologous series”?

A

a family of hydrocarbons with similar chemical properties who share the same general formula

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18
Q

What is a functional group?

A

Functional groups refer to specific atoms bonded in a certain arrangement that give a compound certain physical and chemical properties

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19
Q

What are alkanes?

A
  • Simplest homologous series
  • General formula CnH2n+2
  • Saturated chains of carbon atoms
20
Q

What is meant by the term saturated?

A

All the carbon-to-carbon bonds in the molecule are SINGLE bonds

21
Q

What is the general formula for alkenes?

22
Q

What is the difference between alkanes and alkenes?

A

Alkenes are unsaturated hydrocarbons:
-contain carbon and hydrogen atoms only, but there is at least one carbon-to-carbon bond in the molecule that is a double bond (C=C)

23
Q

What are the rules to naming alkenes?

A
  • The number that indicates the position of the double bond is the lower of the two possible numbers
  • The number is inserted in the name after the prefix and before the suffix.
  • Numbers are separated by “,” and words and numbers and separated with “-“
  • If there is more than one double bond, the suffix -diene, -triene, and so on
  • Each double bond must have a number to indicate its position
24
Q

How do you test for alkenes/ unsaturation?

A
  • Add bromine water/ (if testing a gas, bubble the gas into a solution of bromine water) to the solution you’re testing
  • If an alkene is present, the bromine water changes from orange to colourless
25
What is addition polymerisation?
- During polymerisation, the reactant alkene molecules react with each other to form very long-chain product molecules - The small reactant alkene molecules are unsaturated and are called monomers - One of the bonds in the C=C of the monomer molecules is broken, and C-C bonds are formed end to end between neighbouring monomer molecules - The large product molecule is saturated and is called a polymer
26
How do you draw a monomer?
``` LOOK AT PICTURE ON PHONE -just the compound -No trailing single bonds -Double bond present No brackets -"n" to represent a large number ```
27
How do you draw a repeating unit?
LOOK AT THE PICTURE ON PHONE - No double bond - Trailing single bonds to the 2 C atoms of the double bond - Brackets - "n" to represent a large number
28
What are the conditions for an addition polymerisation reaction?
- High pressure | - Use of catalysts
29
What is condensation polymerisation? How is it different from addition polymerisation reaction?
- A reaction in which small molecules/ monomers join - produce a long-chain molecule/ polymer - The difference is that with condensation polymerisation, there is a byproduct (in addition to the polymer) - Typically H2O or HCl is eliminated every time a linkage is made - Condensation polymerisation also often involves 2 different types of monomer molecules joining together
30
What are the 2 main types of condensation polymers?
- Polyesters | - Polyamides
31
What is the functional group for an ester?
COO
32
What are the 2 functional groups that react to form a polyester?
- A carboxylic acid | - A hydroxyl group of an alcohol
33
What is the functional group for a polyamide?
CONH
34
What are the 2 functional groups that react to form a polyamide?
- A carboxylic group | - An amine group
35
How are proteins made?
- Condensation reaction - b/t amino acids - joined by peptide bonds
36
Describe the structure of an amino acid
consist of: (-NH2) amino group (-COOH) carboxyl group an 'R Group'- this is a side chain that is unique to each amino acid
37
What is meant by the term "biodegradable" when applied to polymers?
- Biodegradable polymers break down (degrade) after their intended use to produce such natural products as: CO2, N2, H2O, etc - This natural breakdown is usually brought about by the action of microorganisms or enzymes - Biodegradable polymers often contain ester or amide linkages
38
What is meant by the term "non-biodegradable"? when applied to polymers?
- Non-biodegradable polymers are NOT broken down after their intended use - Most polymers are of this type and they tend to consist of long chains of carbon and hydrogen atoms - The strong bonding between these atoms makes them resistant to breakdown by microorganisms or enzymes.
39
What is the functional group for alcohols?
-OH
40
What is the general formula for an alcohol?
CnH2n+1OH
41
How does sodium react with alcohols? Use ethanol as an example
2Na+2C2H5OH--->2C2H5ONa + H2 -C2H5ONa (sodium ethoxide) is a strong alkali when aqueous & colourless
42
What is the functional group for carboxylic acids?
-COOH
43
What is the general formula for carboxylic acids?
CnH2n+1COOH
44
How does being a weak acid affect the properties of carboxylic acids?
-They are only partially dissociated into ions when in aqueous solution: RCOOH(aq) ⇌ RCOO−(aq) + H+(aq) -Acids so they: *react with metals to form a salt+H2 *react with bases to form a salt+H2O *react with carbonates to form a salt+H2O+CO2
45
How do carboxylic acids react with alcohols?
-React with alcohols to produce esters (-COO) -Condensation reaction; water is eliminated -Reaction is also reversible -conc H2SO4 is usually used as the acid catalyst -NAMING THE ESTER PRODUCED: *first part comes from alcohol *second part comes from the salt of the carboxylic acid (E.g, ethanoic acid + methanol ---> methyl ethanoate)