Module 2 Chapter 13/14 Flashcards

1
Q

What reagent and condition is needed for an alkene to react to form alcohol

A

Acid catalyst (H3Po4) and steam

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

What is meant by the term structural isomer

A

Same molecular formula but different structural formula

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

Suggest why an alkene is less soluble in water than an alcohol

A

Alkenes do not contain OH groups therefore do not form hydrogen bonds with water

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

What is the mechanism when an alkene reacts with a bromine molecule to produce 1,2,3 tribromopropane

A

Electrophilic addition

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

State what reagent and condition is needed for alkene to form 1-bromopropane

A

Hydrogen and nickel catalyst

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

Radical substitution produces a mixture of organic products.
Suggest 2 reasons why

A

It produces different termination products

Substitution at different positions along the chain

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

What is the general formula for alkyl groups

A

CnH2n+1

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

Iodine monobromide, I-Br, is a polar molecule.
Heterolytic fission of the I-Br bond forms an electrophile.
State the meaning of the term electrophile and suggest the formula of the electrophile formed from IBr

A

Electrophile is electron pair acceptor

I+

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

What does a curly arrow represent in a reaction mechanism

A

Movement of a pair of electrons

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

Cyclopentene can be prepared from cyclopentanol .

What type of reaction is this

A

Elimination reaction

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

Describe the oxidation reactions of Butan-1-ol forming an aldehyde and a carboxylic acid

A

Butan-1-ol can be heated under distillation and the oxidising agent is Cr2O7 2- and the catalyst is an acid - H+.
This produces an aldehyde ; butanal - CH3CH2CH2CHO

Butan-1-ol can also be heated under reflux and the oxidising agent is Cr2O7 2- and the acid catalyst is H+. This produces a carboxylic acid ; but anoxic acid. CH3CH2CH2COOH
this is done by distillation

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

Bromocyclohexane —> E —> cyclohexene

What compound is E and what reagent and conditions is needed

A

Cyclohexane-1-ol

Acid catalyst and heat

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

Why is butan-2-ol classified as a secondary alcohol

A

Butan-2-ol ha 2 R groups ; Ch3 and C2H5

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
14
Q

Give one reason why a Bunsen burner and a beaker is not suitable apparatus for oxidising butan-2-ol

A

Butan-2-ol is flammable and will boil away so you need to head under reflux using a condenser and a pear shaped flask

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
15
Q

At room temperature and pressure, the first four members of the alkanes are all gases but the first four alcohols are all liquids. Explain this difference in terms of intermolecular forces.

A

Alkanes only contain hydrogen and carbon therefore they only have london forces. Alcohols contain OH bonds therefore hydrogen bonds can be made.
Hydrogen bonds are stronger than london forces.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
16
Q

2-methylpropan-1-ol = 108°
Butan-1-ol = 117°
Explain why the boiling points are different

A

2-methylpropan-1-ol has less surface contact. It has fewer london forces compared to butan-1-ol. So less energy is required to break the london forces.

17
Q

Describe a simple test a student can carry out to confirm the presence of an alkene

A

Bromine water should turn from brown to colourless ; decolorisation

18
Q

What observations are made during oxidation of alcohols

A

Should turn orange to green

19
Q

Suggest one advantage of adding cyclohexane to hexane in petrol

A

Cyclohexane will burn more efficiently

20
Q

Explain what is meant by the term stereoisomers

A

Same structural and molecular formula but different arrangement in space

21
Q

Explain how sodium hydrogen carbonate removes hydrogen chloride

A

Sodium hydrogen carbonate neutralises HCL

22
Q

Alkene to alkane what reagents and conditions do u need

A

Hydrogen and nickel catalyst

23
Q

Outline how a catalyst increases the rate of a chemical reaction

A

A catalyst speeds up the rate of reaction by lowering the activation energy so grater proportion of molecules exceed the activation energy

24
Q

Combustion of polymer produced HCL, which is a toxic gas.

Describe how hcl is removed from the waste gases produced

A

HCl is passed through alkali

25
Q

State one advantage of using polymers made from natural foods

A

Biodegradable

26
Q

What is the general formula for alkyl group

A

CnH2n+1

27
Q

Waste polymers are processed to save resources. E.g. by recycling
Describe two other ways in which waste poly(propene) can be processed in a sustainable way

A
  1. Combustion for energy production

2. Use as an organic feedstock

28
Q

Pent-1-ene does not show stereoisomerism

Explain why

A

One of the carbons of the C=C has 2 of the same groups attached

29
Q

Describe one difference between the sigma bond and the pi bond

A

Sigma bond is a head on overlap.

Pi bond is a sideways overlap

30
Q

State and explain the features of a hex-2-ene molecule that lead to E and Z isomers

A

Carbon-carbon double bond does not rotate

Each carbon atom of the double bond attached to 2 different groups

31
Q

State one advantage and disadvantage of using combustion as a method for the disposal of waste polymer 1-dichloro, ethane

A

advantage - energy production which produces electricity

disadvantage - contains Cl which produces HCl a toxic gas which can cause acid rain

32
Q

A student reacts pent-2-ene with bromine in the laboratory.

What does It form?

A

D - 2,3-dibromopentane