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A Level Chemistry 9701 (Chap 27,28)(Nitrogen Compounds,Polymers)

Total questions: 20

Worksheet time: 27mins

Name
Class
Date
1.

Which one is the weakest base?

a)

Ethylamine

b)

Methylamine

c)

Ammonia

d)

Phenylamine

2.

A student wants to prepare ethylamine (a primary amine) with the help of the given reaction but he risks forming secondary and tertiary amines. Choose the right set of conditions for him to work.

a)

Excess conc. ammonia solution

b)

Excess conc. ethanolic ammonia

c)

Excess conc. ethanolic ammonia with heat

d)

Excess conc. ethanolic ammonia with heat and pressure

3.

A student wants to prepare the compound shown; diethylamine (a secondary amine). Choose the right set of reactants and conditions for him to work.

a)

Ethylamine reacting with ethyl bromide under heat

b)

Ethylamine reacting with ethyl bromide under heat and pressure

c)

Excess conc. ethanolic ammonia with heat reacting with ethyl bromide

d)

Excess conc. ethanolic ammonia with heat and pressure reacting with ethyl bromide

4.

A student wants to make ethylamine with a 2 step process. Choose the correct step 1 and step 2 for a successful process. (This question requires you to choose 2 correct options out of 4)

a)

Step 1: Convert halogenoalkane to Alkane nitrile

b)

Step 1: Convert aldehyde to Alkane nitrile

c)

Step 2: Convert Alkane nitrile to Ehtylamine by the process of reduction

d)

Step 2: Convert Alkane nitrile to Ethylamine by the process of alkaline hydrolysis

5.

How can you convert amides to primary amines?

a)

Reduction with LiAlH4 in dry ether

b)

Reduction with NaBH4 in aqueous conditions

c)

Acidic Hydrolysis

d)

Alkaline Hydrolysis

6.

A student wanted to prepare phenylamine with the given process. He carried out a reduction reaction by heating nitrobenzene under the reflux with Tin (Sn) and concentrated hydrochloric acid. Instead of getting phenylamine, the resulting acidic mixture gave him the ion C6H5N+H3 and he did not know what to do next. Choose the right step for him.

a)

Add HCl and then steam distill

b)

Just steam distill

c)

Just add NaOH

d)

Add NaOH and then steam distill

7.

What is the color of the precipitate in the given example?

a)

Red-brown ppt

b)

Blue-black ppt

c)

White ppt

d)

First yellow then brown after 10-15 minutes

8.

Properly name the steps 1 and 2. (This questions requires you to choose 2 correct options out of 4)

a)

Step 1: Diazotisation

b)

Step 1: Aromatisation

c)

Step 2: Coupling Reaction

d)

Step 2: Diaozotisation

9.

The reaction mixture is supposed to be kept below 10ₒC because:

a)

Nitrous Acid does not react at higher temperatures

b)

The diazonium ion is converted to a diazonium salt

c)

The diazonium ion reacts with the negative nitrate (III) ions in the reaction mixture to form another product

d)

The diazonium ion is unstable and decomposes easily to give off nitrogen gas

10.

What is the correct general structural formula of an amino acid (2-aminocarboxylic acid)?

a)

RCH(NH2)COOH

b)

RCH2(NH)COOH

c)

R1R2C(NH2)COOH

d)

R3C(NH2)COOH

11.

The pH value at which there is no overall charge on a particular amino acid in its aqueous solution is known as _____________.

a)

Neutrality Point

b)

Neutralisation Point

c)

Electric Point

d)

Isoelectric Point

12.

What kind of reaction is the formation of an amide bond (peptide linkage) between two amino acids for a dipeptide formation?

a)

Condensation Reaction

b)

Addition Reaction

c)

Elimination Reaction

d)

Polymerisation Reaction

13.

Why are acyl chlorides preferred over carboxylic acids for the formation of amides such as ethanamide?

a)

Carboxylic Acids are more reactive than acyl chlorides and gives too many side products

b)

Carboxylic Acids are more acidic than acyl chlorides and give acidic salts as product instead of the original required product

c)

Acyl chlorides are more reactive than carboxylic acids

d)

Acyl chlorides are cheaper (inexpensive) as compared to carboxylic acids

14.

If excess of acid is taken, then pick the correct set of final products:

a)

Acidic Hydrolysis Products: R1COOH + R2NH3+

Alkaline Hydrolysis Products: R1COO-Na+ + R2NH2

b)

Acidic Hydrolysis Products: R1COOH + R2NH2

Alkaline Hydrolysis Products: R1COO-Na+ + R2NH2

15.

Both of the given polymers come from the same monomer. Choose the monomer correctly.

a)

Ethene

b)

Ethyne

c)

Cis-Ethyne

d)

Trans-Ethyne

16.

How many water molecules does the formation reaction of this tripeptide will give?

a)

Zero

b)

1

c)

2

d)

3

17.

If Nylon 6,6 is prepared from 1,6-diaminohexane [H2N(CH2)6NH2] and hexanedioyl dichloride [ClOC(CH2)4COCl], what other product will one get?

a)

H2O

b)

HCl

c)

NH3

d)

Just the polymer, no other products

18.

Generally Kevlar can be created by reacting the following: (Select all that apply)

a)

An aminobenzene with a benzene based carboxylic acid

b)

A diaminobenzene with a benzene dicarboxylic acid

c)

A diaminobenzene with a benzene dioyl dichloride

d)

An aminobenzene with an acyl chloride

19.

Write the IUPAC name of the monomer that forms this polymer.

a)

2-hydroxypropanoic acid

b)

3-hydroxypropanoic acid

c)

2-methanol propanoic acid

20.

Terylene is a polymer that is usually made from benzene-1,4-dicarboxylic acid and one more organic monomer under specific reaction conditions including catalyst. Name the other organic monomer.

a)

Ethane-1,2-diol

b)

Ethane-1,1-diol

c)

Propane-1,3-diol

d)

Propane-1,2-diol