Biochemistry reactions Flashcards

1
Q

Describe the three steps of radical substitution.

A
  1. Initiation
    -The production of free radicals.
  2. Propagation
    -The steps which produce products and more
    free radicals.
  3. Termination
    -Two free radicals meet to form a product.
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
2
Q

Describe the difference between homolytic and heterolytic fission.

A

Homolytic fission involves the breaking of a covalent bond where both atoms leave with one electron from the shared pair.
Heterolytic fission is where one atom takes both electrons because it is more electronegative.

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

What mechanism is involved in halogenation of alkenes?

A

Electrophilic addition

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

Describe two sets of conditions needed for cracking.

A
  1. High temperate and high pressure

2. Lower temperature and ZEOLITE catalysts

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

Describe the reactants, products, and the necessary catalyst for hydration of an alkene.

A

Addition of water to an alkene, forming an alcohol. Catalyst of sulphuric acid / phosphoric acid.

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

Describe the necessary conditions, reactants and products formed for hydrogentation of alkenes.

A

Addition of hydrogen.
Catalyst such as nickel or platinum.
Product is corresponding alkane.
Conditions - around 4 atm at 150-250 degrees celcius.

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

What reactant is used in the oxidation of alkenes to diols?

A

Cold dilute, acidified solution of potassium permanganate.

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

What reactant is used for the further oxidation of diols to carboxylic acids or ketones?

A

Hot concentrated, acidified solution of potassium permanganate.

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

In the oxidation of diols with hot concentrated acidic potassium permangante, a single carbon fragment will yield what oxidised product?

A

Carbon dioxide.

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

In the oxidation of diols with hot concentrated acidic potassium permangante, a primary alcohol fragment will yield what oxidised product?

A

Carboxylic acid.

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

In the oxidation of diols with hot concentrated acidic potassium permangante, a secondary alcohol fragment will yield what oxidised product?

A

Ketone.

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

What is the mechanism involved in addition polymerisation?

A

Free radical.

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

Describe two methods of producing methanol.

A
  1. Hydrogenation of carbon monoxide with synthesis gas (200-300 degrees, 100 atm H2 gas) over a copper catalyst.
  2. Dry distillation of wood.
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
14
Q

Describe a method of producing ethanol.

A

Fermentation of sugar using yeast enzyme.

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

How can any alcohol be formed?

A

From the hydration of alkenes using a catalyst of concentrated phosphoric acid.

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

What are the products of combustion of alcohols?

A

Water and carbon dioxide.

17
Q

What are the two most common oxidising agents for alcohols?

A

Acidified potassium dichromate and acidified potassium permanganate.

18
Q

What are some steps necessary to obtain a desired product of aldehyde when oxidising a primary alcohol, and how is it possible?

A

Use a mild oxidising agent (acidified potassium dichromate) / limited oxidising agent / excess alcohol and DISTILLATION. Aldehydes have low boiling points because of no hydrogen bonding.

19
Q

What will be the product of oxidising a secondary alcohol?

A

Ketone.

20
Q

What will be the product of oxidising a tertiary alcohol.

A

No product. Tertiary alcohols cannot be oxidised.

21
Q

What are the colour changes for two reagents which show a positive test for the oxidisation of a primary or secondary alcohol?

A

Acidified potassium dichromate - orange to green

Acidified potassium permanganate - purple to colourless

22
Q

What must be present in an alcohol&raquo_space; haloalkane substitution reaction for it to take place?

A

A strong acid.

23
Q

What is the product formed and catalyst required for a dehydration of an alcohol.

A

Alkene. Acid catalyst.

24
Q

Describe the steps to obtain an ester from an alcohol and a carboxylic acid. Name this reaction.

A

Esterification of alcohol with carboxylic acid. Requires concentrated sulfuric acid catalyst and reflux (because it is an equilibrium reaction).

25
Q

What is the main difference in terms of numbers of steps between SN1 and SN2 reactions?

A

SN1 reactions happen in two steps and SN2 happens in 1 step.

26
Q

What is Markovnikov’s rule?

A

The hydrogen atom in an HX compound bonds to the carbon with the most number of hydrogen atoms around it.

27
Q

What two reducing agents are used for the reduction of aldehydes or ketones to alcohols?

A

NaBH4, or LiAlH4 dissolved in ethanol.

28
Q

What type of reaction the is addition of HCN to aldehydes or ketones?

A

Nucleophilic addition.

29
Q

How can ammonia be obtained from an aldehyde / ketone?

A

Nucleophilic addition of HCN to aldehyde / ketone to create a hydroxynitrile. Then hydrolysis of the hydroxynitrile to form a carboxylic acid and ammonia.

30
Q

What test can be run for the presence of a carbonyl group?

A

Addition of 2,4-DNPH. Formation of orange ppt indicates carbonyl group.

31
Q

What tests indicated the presence of an aldehyde.

A

Fehling’s solution - reduced to red ppt.

Tollen’s reagenet - ‘silver mirror’ effect upon heating.

32
Q

How can a nitrile be obtained from an alkyl halide?

A

Nucleophilic substitution of an aklyl halide with NaCN / KCN dissolved in ethanol.

33
Q

How can an amine be obtained from an alkyl halide?

A

When an alkyl halide is reacted with ammonia dissolved in ethanol.

34
Q

How can an alcohol be obtained from an alkyl halide?

A

Hydrolysis of an alkyl halide with a mixture of water and ethanol.

35
Q

How can an alkene be obtained from an alkyl halide?

A

Elimination reaction when an alkyl halide is reacted with KOH / NaOH dissolved in ethanol.

36
Q

What solid catalyst can be used for the dehydration of an alcohol?

A

Aluminium oxide.