CONCORDIA COLLEGE KASUR Test # 5 A

CLASS 2ND YEAR SUBJECT CHEMISTRY DATE TOTAL MARKS 30

ROLL NO. STUDENT NAME TIME ALLOWED 50 Min
SYLLABUS CH# 10+13 
Q.No.1 Choose the correct option: (1×10=10)
1. In secondary alkyl halides, halogen is attached to that carbon atom which is further
attached to how many hydrogen atoms?
(A) 1 (B) 2 (C) 3 (D) 4
2. Which one of the following is not a nucleophile?
(A) H2O (B) H2S (C) NH3 (D) BF3
3. What will be the mechanism of the reaction? C2H5I + 2NH3 C2H5NH2 + NH4I
(A) SN1 (B) SN2 (C) E2 (D) E1
4. Common name of 2-Chloro-2-methylpropane is
(A) iso-butyl chloride (B) sec-butyl chloride
(C) ter-butyl chloride (D) n-butyl chloride
5. Which one of the following is best nucleophile?
(A) H2O (B) NO (C) NH3 (D) C2H5O-
6. Which of the following acid is used to prepare synthetic fibre?
(A) formic acid (B) carbonic acid (C) acetic acid (D) butyric acid
7. Which reagent is used to reduce carboxylic acid to an alkane?
(A) Ni/H2 (B) Pd/H2 (C) P/HI (D) LiAlH4
8. A carboxylic acid contains
(A) a hydroxyl group (B) a hydroxyl and carbonyl group
(C) a carbonyl group (D) a carboxyl and aldehydic group
9. Which of the following is not a fatty acid?
(A) acetic acid (B) butanoic acid (C) propanoic acid (D) phthalic acid
10. Acetamide is prepared by
(A) heating ammonium carbonate (B) heating methyl cyanide
(C) heating ethyl acetate (D) hydrolysis of methyl cyanide
 
Q.No.2. Write short answers to the following questions. (6×2=12)
i) Describe Wurtz reaction.
ii) Prepare ethyl thioalcohol and ethyl acetate from ethyl bromide.
iii) How does Grignard reagent react with epoxides?
iv) Discuss reactivity of alkyl halide on the basis of bond energy.
v) Write down mechanism of SN2 reaction.
vi) How is 1-chloropropane reduced to get propane?
vii) What are neutral amino acids?
viii) Write down Strecker method for amino acid preparation.
Note: Attempt the following Questions. (8×1=8)
Q.No.3
(a) What is Grignard reagent? How does it react with carbonyl compounds? (4)
(b) Discuss mechanism of formation of acetyl chloride from thionyl chloride. (4)
 CONCORDIA COLLEGE KASUR Test # 5 A
CLASS 2ND YEAR SUBJECT CHEMISTRY DATE TOTAL MARKS 30
ROLL NO. STUDENT NAME TIME ALLOWED 50 Min
SYLLABUS CH# 10+13 

Q.No.1 Choose the correct option: (1×10=10)

1. Which of the following acid is used to prepare synthetic fibre?
(A) formic acid (B) carbonic acid (C) acetic acid (D) butyric acid
2. Which reagent is used to reduce carboxylic acid to an alkane?
(A) Ni/H2 (B) Pd/H2 (C) P/HI (D) LiAlH4
3. A carboxylic acid contains
(A) a hydroxyl group (B) a hydroxyl and carbonyl group
(C) a carbonyl group (D) a carboxyl and aldehydic group
4. Which of the following is not a fatty acid?
(A) acetic acid (B) butanoic acid (C) propanoic acid (D) phthalic acid
5. Acetamide is prepared by
(A) heating ammonium carbonate (B) heating methyl cyanide
(C) heating ethyl acetate (D) hydrolysis of methyl cyanide
6. In secondary alkyl halides, halogen is attached to that carbon atom which is further
attached to how many hydrogen atoms?
(A) 1 (B) 2 (C) 3 (D) 4
7. Which one of the following is not a nucleophile?
(A) H2O (B) H2S (C) NH3 (D) BF3
8. What will be the mechanism of the reaction? C2H5I + 2NH3 C2H5NH2 + NH4I
(A) SN1 (B) SN2 (C) E2 (D) E1
9. Common name of 2-Chloro-2-methylpropane is
(A) iso-butyl chloride (B) sec-butyl chloride
(C) ter-butyl chloride (D) n-butyl chloride
10. Which one of the following is best nucleophile?
(A) H2O (B) NO (C) NH3 (D) C2H5O-
Q.No.2. Write short answers to the following questions. (6×2=12)
i) Write down mechanism of SN2 reaction.
ii) How is 1-chloropropane reduced to get propane?
iii) What are neutral amino acids?
iv) Write down Strecker method for amino acid preparation.
v) Why carboxylic acids have high boiling points than alcohols?
vi) Convert acetic acid into ethanol.
vii) Write down formula of tartaric acid and lactic acid.
viii) What is peptide bond? Write down formula of dipeptide. 
Note: Attempt the following Questions. (8×1=8)
Q.No.3
(a) Write a note on SN1 reaction. (4)
(b) Discuss four methods for the preparation of carboxylic acids. (4)