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Worksheets

MRE_Yr 13 Organic Revision

Total questions: 73

Worksheet time: 2hrs 26mins

Name
Class
Date
1.
The molecular formula for Heptane is
a)
C4H10
b)
C8H18
c)
C5H12
d)
C7H16
2.
Which of the following could contain a triple bond?
a)
C4H10
b)
C4H8
c)
C4H6
d)
C4H12
3.

A homologous series is a family of organic compounds with

a)

similar chemical properties and same general formula as found on Table Q

b)

different chemical properties and different general formula as found on Table P

4.

Which is the structures with IUPAC nomenclature


2,2,4-trimethylpentane

a)
b)
c)
d)
5.
a)
2,3-dimethyl-4,4-diethyl heptane
b)
2,3-methyl-4,4-ethyl heptane
c)
4,4-ethyl-2,3-methyl heptane
d)
4,4-diethyl-2,3-dimethyl heptane
6.
How many carbons are in the longest chain of the following molecule:
a)
11
b)
10
c)
9
d)
8
7.

Which the CORRECT reagent and condition for A

a)

HBr

b)

Cl2, H2O

c)

H2, Ni

d)

HBr, H2O2

8.

Deduce the structure for C

a)
b)
c)
d)
9.

Nucleophiles are

a)

electron pair donors that attack regions of high electron density.

b)

electron pair donors that attack regions of low electron density.

c)

electron pair acceptors that attack regions of high electron density.

d)

electron pair acceptors that attack regions of low electron density.

10.

Which of these compounds is a secondary halogenoalkane?

a)

CH3CH(OH)CH3

b)

CH3CCl(CH )CH3

c)

CH3CHClCH3

d)

CH3CH2 CH2 Cl

11.

Which one of the following will undergo nucleophilic substitution with sodium hydroxide (aq)?

a)

ethene

b)

ethane

c)

bromoethane

d)

cyclopentane

12.

what is the mechanism of the reaction when sodium hydroxide in ethanolic condition reacts with cloroethane under reflux?

a)

nucleophilic substitution

b)

electrophilic addition

c)

free radical substitution

d)

elimination

13.

Which of the following is not the product of elimination reaction between ethanolic sodium hydroxide and chloroethane?

a)

sodium chloride

b)

water

c)

ethene

d)

hydrogen chloride gas

14.

Why does the reaction

C2H5X + OH- → C2H5OH + X-

occur faster if X is iodine instead of Bromine?

a)

the I- ion is a stronger nucleophile than the Br- ion.

b)

the I- ion is less hydrated in water than the Br- ion

c)

C-Br bond is more polar than the C-I bond

d)

the C-Br bond is stronger than the C-I bond

15.

What type of organic product is formed from the oxidation of a secondary alcohol?

a)

Carboxylic acid

b)

Aldehyde

c)

Ketone

d)

Alkene

16.

Fehling's reagent shows the following colour change when added to an aldehyde

a)

Colourless to silver mirror

b)

Brick red to blue

c)

Stays blue

d)

Blue to brick red

17.

Dehydration of an alcohol gives

a)

an aldehyde

b)

an alkane

c)

an alkene

d)

a ketone

18.

Fehling's reagent shows the following colour change when added to a ketone

a)

Blue to brick red

b)

Colourless to silver mirror

c)

Stays blue

d)

Silver to colourless

19.

Oxidising reagents are represented by the following symbol in equations

a)

OH-

b)

O

c)

[O]

d)

Ox.

20.

What charge do the orange potassium dichromate ions have?

a)

+3

b)

-6

c)

+6

d)

-3

21.

When reacted with a strong reducing agent, aldehydes turn into

a)

primary alcohols

b)

secondary alcohols

c)

ketones

d)

carboxylic acids

22.

Classify the compound based on the functional group present.

a)

aldehyde

b)

carboxylic acid

c)

ketone

d)

alcohol

23.

The class of compounds containing C=O are called

(a)  

24.

How could you prepare this compound: (propanal)?

         

a)

Reduce

butanoic acid

b)

Oxidize

propan-2-ol

c)

Oxidize

propan-2-one

d)

Oxidize

propan-1-ol

25.

Two physical properties of aldehydes are:

a)

They can form hydrogen bonds

b)

Higher boiling points than hydrocarbons and alcohols of similar molecular weight.

c)

Higher boiling points than hydrocarbons; but  lower than alcohols of similar molecular weights.

d)

Aldehydes with high molecular weight are soluble in water.

26.

What will be formed if butanone is reacted with LiAlH4 in dry ether?

a)

Butanoic acid

b)

Butan-1-ol

c)

Butan-2-ol

d)

Butanal

27.

What is the name of the mechanism when KCN (in acidic conditions) reacts with propanal?

a)

Free radical substitution

b)

Nucleophilic substitution

c)

Nucleophilic addition

d)

Electrophilic addition

28.

Boiling points of carboxylic acids is higher than those of corresponding alcohols.


Is the above statement True or False?

a)

True

b)

False

29.

Which is the correct IUPAC name of the following compound?

a)

A. 2-hydroxybutanoic acid

b)

B. 3-hydroxybutanoic acid

c)

C. 2-hydroxypropanoic acid

d)

D. 1-carboxypropan-2-ol

30.

Reaction of a carboxylic acid and sodium hydroxide will produce:

a)

a substituted ammonium salt

b)

a substituted carbonate salt

c)

a substituted water

d)

a substituted carboxylates

31.

What is the suffix for carboxylic acids?

a)

-ic acid

b)

-oic acid

c)

-oic

32.

The reaction between HCOOH and CH3COOH produces an ester called methyl methanoate.

a)

True

b)

False

33.

The molecular formula of pentanoic acid is

a)

C5H11O2

b)

C5H9O2

c)

C5H10O2

d)

C5H12O2

34.

What is the correct IUPAC name for the Carboxylic Acid shown?

a)

1,1,1-trimethylbutanoic acid

b)

1,1,1-trimethylpentanoic acid

c)

4,4-dimethylbutanoic acid

d)

4,4-dimethylpentanoic acid

35.

The diagram shows the partial structure of Terylene. From which pair of compounds is it made?

a)
b)
c)
d)
36.

What is the partial structure of the polymer formed by the polymerisation of propene, CH3CH=CH2?

a)
b)
c)
d)
37.

Which of the following is not a primary amine?

a)

Diethylamine

b)

3-Hexylamine

c)

Cyclohexylamine

d)

1-Butylamine

38.

Which statement about the reaction of 1-bromobutane and NH3 is incorrect?

a)

The reaction may lead to the formation of a quaternary ammonium salt

b)

The reaction initially gives a primary amine

c)

The reaction is a nucleophilic substitution

d)

The reaction specifically gives a primary amine

39.

Which of the following amines do you expect to have the highest boiling point?

a)

Triethyl amine

b)

methyl amine

c)

dimethyl amine

d)

diethyl amine

40.

Which of the following compound is commonly used as cationic surfactant in fabric softening

a)

Quaternary ammonium salt

b)

tertiary amine

c)

primary amine

d)

amide

41.

Which one among the following is a strongest base

a)

methyl amine

b)

Ammonia

c)

Phenyl amine

42.
a)

N-ethyl-N-methylpropanamide

b)

N-ethyl-N-methylbutanamide

c)

N-methyl-N-propylethanamide

d)

N,N-dimethylpropanamide

43.

This compound is an example of

a)

a primary amine

b)

a secondary amine

c)

a tertiary amine

d)

cannot be classified as a primary, secondary or tertiary amine

44.

What is the reagent required to carry out the following conversion?


Hexanamide --> hexanamine

a)

NaOH

b)

Dilute HCl

c)

HNO2

d)

LiAlH4, ether

45.

What is the reagent required to carry out the following conversion?


Methylamine --> N-methylethanamide

a)

NaOH

b)

Methanoyl chloride

c)

HNO2

d)

Ethanoyl chloride

46.

What is the basis for classifying amines as primary, secondary, or tertiary?

a)

the number of carbon atoms bonded directly to the nitrogen atom

b)

the number of carbon atoms bonded to a carbon bearing nitrogen

c)

the number of nitrogen atoms present

d)

the number of hydrogen atoms present

47.

Which one is a neutral amino acid with non-polar side chain?

a)
b)
48.

Which one is a basic amino acid?

a)
b)
49.

Which one has more than one chiral center?

a)
b)
50.

Are these statements about amino acids true or false?

In the solid state amino acids exists as zwitterions

a)

true

b)

false

51.

Are these statements about amino acids true or false?

Amino acids undergo addition polymerisation to form polypeptides

a)

true

b)

false

52.

Are these statements about amino acids true or false?

Peptide links can undergo hydrolysis by reflux with hydrochloric acid

a)

true

b)

false

53.

What's the correct definition of these keywords?

zwitterions

a)

Amino acid molecules with a negative charge on the amine group in the form of COO- and a positive charge on the carboxylic acid group in the form of NH3+

b)

Amino acid molecules with a positive charge on the amine group in the form of NH3+ and a negative charge on the carboxylic acid group in the form of COO-

c)

Amino acid molecules with a negative charge on the amine group in the form of NH3- and a positive charge on the carboxylic acid group in the form of COO+

54.

What's the correct definition of these keywords?

polyamide

a)

An addition polymer formed from a dicarboxylic acid and a diol

b)

An condensation polymer formed from a dicarboxylic acid and a diol

c)

An condensation polymer formed from a dicarboxylic acid and a diamine

55.

Which of these structures is a zwitterion?

a)
b)
c)
56.

The structure below is the amino acid valine. What is its structure when in a solution of high pH?

a)
b)
c)
57.

The stucture below is the amino acid glycine. What is its structure when two glycine molecules form a peptide bond?

a)
b)
c)
58.

2-Methylbutylamine can be synthesised from an alkene.


What is the identity of the alkene?

a)

But-2-ene

b)

Methylpropene

c)

2-Methylbut-1-ene

d)

2-Methylbut-2-ene

59.

Which one of the following pairs of reagents reacts to form an organic product that shows only 2 peaks in its proton n.m.r. spectrum?

a)

butan-2-ol and acidified potassium dichromate(VI)

b)

ethanoyl chloride and methanol

c)

propanoic acid and ethanol in the presence of concentrated sulphuric acid

d)

ethene and hydrogen in the presence of nickel

60.

Which one of the following pairs reacts to form an organic product with only 2 singlets in its proton n.m.r. spectrum?

a)

ethene and bromine

b)

propan-2-ol and acidified potassium dichromate(VI)

c)

ethanol and concentrated sulphuric acid

d)

epoxyethane and water in the presence of dilute sulphuric acid

61.

Which one of the following types of reaction mechanism is not involved in the above sequence?

a)

free-radical substitution

b)

nucleophilic substitution

c)

elimination

d)

nucleophilic addition-elimination(

62.

Refer to the following reaction sequence:


Which one of the following types of reaction is not involved in the above sequence?

a)

acylation

b)

oxidation

c)

reduction

d)

dehydration

63.

How many carbon environments?2

a)

1

b)

2

c)

4

d)

6

64.

How many carbon environments?

a)

1

b)

2

c)

3

d)

4

65.

How many carbon environments?

a)

2

b)

3

c)

4

d)

5

66.
Which molecule will produce the following spectra with 3 different H environment?
a)
CH3CH2CH2CH3
b)
CH3CH2CH3
c)
CH3COCH2CH3
d)
CH3COOCH2CH3
67.
Which molecule will produce the following spectra with one H environment?
a)
CH3CH2CH3
b)
CH3COOCH3
c)
CH3CH3
d)
CH3COCH3
68.

Which of the following would not give singlet signal in NMR?

a)

Ethane

b)

Dimethylether

c)

Diethylether

d)

Acetone

69.

How many NMR signals would be given by the compound (CH3)2CHCH2CH3

a)

1

b)

2

c)

3

d)

4

70.
A sample of pure chlorine gas is analyzed in the MS. Which of the following is a correct interpretation?
a)
Chlorine has an isotope with a mass of 70 amu
b)
Chlorine has three known isotopes
c)
Chlorine is diatomic
d)
Chlorine is highly reactive
71.

If the molecular ion, M+ m/z = 136 and M+2+ at m/z = 138 of approximately equal intensity, which molecule is it?

a)

C6H13OCl

b)

C10H16

c)

C9H12O

d)

C4H9Br

72.

The amount of energy in infrared light corresponds to:

a)

the amount of energy needed to promote one electron from a

bonding to an antibonding molecular orbital

b)

the amount of energy needed to increase certain molecular

motions, such as bond vibrations, in organic molecules

c)

the amount of energy needed to strip a molecule of one electron to generate a cation radical

d)

the amount of energy needed to "flip" the spin of a 13C or 1H nucleus

73.

Examining the infrared spectrum of a compound allows us to:

a)

determine the types of functional groups present in the compound

b)

determine the nature of the conjugated pi electron system in the compound

c)

determine the molecular weight of the compound

d)

determine the carbon-hydrogen framework of the compound