Exam Cards - Unit 2: Basic Concepts & Hydrocarbons Flashcards

1
Q

What is the general formula for alkanes?

A

CnH2n + 2

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
2
Q

Define structural isomerism.

A

When molecules have the same molecular formula, but have different structural formulas.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
3
Q

Name and define the three types of structural isomers.

A

Chain isomers - the carbon skeleton is arranged differently Positional isomers - The functional group is arranged in a different position Functional group isomers - The atoms of a functional group can be arranged into a different functional group

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
4
Q

Define stereoisomerism.

A

When molecules have the same structural formula, but arranged differently in space.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
5
Q

Define E/Z isomerism/cis-trans isomerism.

A

When an alkene molecule has an E-isomer and a Z-isomer. E-isomers have the same groups across the double bond, whereas Z-isomers have the same groups both above or both below the double bond.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
6
Q

How is the percentage yield of a reaction calculated?

A

Percentage yield = actual yield/theoretical yield x 100

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
7
Q

How is the theoretical yield calculated?

A

Number of moles (of reactant) x M (of product)

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
8
Q

How is atom economy calculated?

A

molecular mass of useful product/sum of molecular masses of all products x 100

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
9
Q

Why is the atom economy always 100% for addition reactions?

A

The reactants always form a single product.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
10
Q

Why do branched-chain alkanes have lower boiling points than straight-chain alkanes?

A

The smaller molecular surface area of branched-chain alkanes means that they can’t pack closely together, reducing the van der Waals forces.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
11
Q

What are the products of the combustion of an alkane?

A

Carbon dioxide and water.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
12
Q

What are the products of the combustion of alkanes in limited oxygen?

A

Carbon monoxide and water.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
13
Q

Outline fractional distillation.

A
  • Crude oil is vaporised in a fractionating column
  • The vaporised crude oil rises through the column
  • As the oil rises it condenses
  • Each fraction condenses at different levels
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
14
Q

Outline catalytic cracking.

A
  • Heavier fractions are passed over a catalyst at a high temperature
    • THis breaks them into smaller molecules
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
15
Q

Define heterolytic fission.

A
  • One of the bonded atoms takes both of the shared pair of electrons
  • Two ions are produced
  • The atom that took both shared electrons becomes an anion
  • The atom the didn’t take the electrons becomes a cation
  • X-Y -> X+ + Y-
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
16
Q

Define homolytic fission.

A
  • Each bonded atom takes one of the shared pair of electrons
  • Each atom then has an unpaired electron (radical)
  • Two species of the same type are produced
  • X-Y -> X. + Y.
17
Q

What are the prefixes for halogenoalkanes?

A

Fluoro-, Chloro-, Bromo-, or Iodo-.

18
Q

What are the three steps in the reaction mechanism of forming halogenoalkanes?

A
  1. Initiation
  2. Propagation
  3. Termination
19
Q

What happens in the initiation step for the chlorination of methane?

A
  • A Cl-Cl bond is broken by homolytic fission, using energy from UV radiation
  • Two chlorine radicals are formed
20
Q

What happens in the propagation steps for the chlorination of methane?

A
  • Cl. attacks a methane molecule - Cl. + CH4 -> .CH3 + HCl
  • The new methyl free radical can attack another Cl2 molecule - .CH3 + Cl2 -> CH3Cl + Cl.
  • The new Cl. can attack another methane molecule
  • These steps repat until all the Cl2 or CH4 molecules are wiped out
21
Q

What happens in the termination step for the chlorination of methane?

A

Two radicals combine to form a molecule. There are a number of possible combinations.

  • Cl. + Cl. -> Cl2
  • .CH3 + .CH3 -> C2H3
  • .CH3 + .Cl -> CH3Cl
22
Q

What is the equation for the chlorination of methane?

A

CH4 + Cl2 -> CH3Cl + HCl

23
Q

Define standard enthalpy change of reaction.

A

The enthalpy change when the reaction occurs in the molar quantities shown in the chemical equation.

24
Q

Define standard enthalpy change of formation.

A

The enthalpy change when 1 mole of a compound is formed from its elements.

25
Q

Define standard enthalpy change of combustion.

A

The enthalpy change when 1 mole of a substance is completely burned in oxygen.