R2O2/hvHBr(A);   

 

Major product (A) is:

(a) 

(b) 

(c) 

(d) 

Subtopic:  Alkanes, Alkenes and Alkynes - Chemical Properties |
 69%
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What type of product will be formed in the following reaction?


1. A mixture of diastereomers  
2. Optically active
3. A pure enantiomer with 100% optical purity
4. A racemic mixture

Subtopic:  Alkanes, Alkenes and Alkynes - Chemical Properties |
 51%
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 H+Possible products Br2/CCl4(y) products

The number of possible products for x and y is:

(a) 2,4

(b) 3,5

(c) 3,6

(d) 3,4

Subtopic:  Aliphatic Hydrocarbon - Methods of Preparation |
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Product (C) of the above reaction is :

1. 1,3-Hexadiene
2. 1,4-Pentadiene
3. 1,3-Butadiene
4. 1,3-Heptadiene

Subtopic:  Aromatic Hydrocarbons - Benzene - Structure, Preparation & Chemical Reactions |
 53%
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Which reagents are suitable to accomplish the mentioned conversion?

1. O3/H2O2, HO-/                               

2. HBr, alc. KOH, O3, LiAlH4, H+/

3. HBr, t-BuOK, O3, KMnO4

4. HBr, alc. KOH, O3, KMnO4

Subtopic:  Aliphatic Hydrocarbon - Methods of Preparation |
 64%
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0°CPCl5A70-80%(2) H(1) 3NaNH2, mineral oilB46%; Product (B) is:

Subtopic:  Aliphatic Hydrocarbon - Methods of Preparation | Alkanes, Alkenes and Alkynes - Chemical Properties |
 64%
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Product (K) of the above reaction is:

1. 

2. 
3. 

4. 

Subtopic:  Aliphatic Hydrocarbon - Methods of Preparation |
 61%
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CH3-CH2-CH2-CCH+LiHN2(A)(CH3)2SO4(B)

Give the structural formula of compound (B):

(a) CH3-(CH2)2-CC-SO3H

(b) CH3-(CH2)2-CC-CH3

(c)  CH3-(CH2)2-CC-CH2-O-OsO-H

(d) CH3-CH2-CC-CH2

Subtopic:  Aliphatic Hydrocarbon - Methods of Preparation |
 51%
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The reagents used for the following conversion is/are-

 

1. (i) NaNH2 , (ii) CH3CHO
2. (i) NaNH2 , (ii) CH3-CH2-CH2-Br
3. (i) KOH, (ii) CH3-CH2-CH2-Br
4. (i) KOH, (ii) 

Subtopic:  Aliphatic Hydrocarbon - Methods of Preparation |
 81%
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Which alkyne(s) will yield 3-ethylhexane upon catalytic hydrogenation?
 

1.  2. 
3.  4.  All of the above
Subtopic:  Aliphatic Hydrocarbon - Methods of Preparation |
 66%
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