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Which compound/compounds is/are optically active?

1.                        2.  

3.         4.  All of these

Subtopic:  Stereo Isomers |
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Level 1: 80%+
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If 'A' and 'B' are major products then 'B' is

1.        2.  

3.             4.  

Subtopic:  Isomers & Reaction Mechanism |
Level 3: 35%-60%
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Formed product was given

(1)  Ceric ammonium nitrate and NaHCO3 test

(2)  NaHCO3 test and DNP test

(3)  NaHCO3 and Victor Meyer test

(4)  Both (A) & (C)

Subtopic:  Aldehydes & Ketones: Preparation & Properties |
Level 3: 35%-60%
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 Product of products

1.  R - COOH only

2.  R - CHO on;y

3.  R - CHO and R - COOh

4.  

Subtopic:  Aldehydes & Ketones: Preparation & Properties |
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In major product of reaction, how many secondary alcoholic groups are attached to the ring?

1.  Three

2.  Four

3.  Two

4.  One

Subtopic:  Aldehydes & Ketones: Preparation & Properties |
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An organic compound (A) of the molecular formula C6H12O3 gives a positive Iodoform test but does not reduce Tollen's reagent. When (A) is subjected to acid-catalyzed hydrolysis, another compound B is formed which gives positive Tollen's test. Identify the unknown compound (A).

1.       

2.  

3.  

4.  

Subtopic:  Aldehydes & Ketones: Preparation & Properties |
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Level 3: 35%-60%
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PH - CHO CH3COONa/H2OCH3 - CO2OA 
The prodct A is

1.        2.   

3.          4.  

Subtopic:  Aldehydes & Ketones: Preparation & Properties |
 58%
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The product (A) from this reaction has the potential to show:
\(\mathrm{C}_2 \mathrm{H}_4 \xrightarrow{\mathrm{O}_3 / \mathrm{Zn} / \mathrm{H}_2 \mathrm{O}_2} \text { Product } \mathrm{A}\)



1. Haloform test

2. Aldol condensation

3. Cannizzaro reaction

4. Both (1) & (2)

Subtopic:  Aldehydes & Ketones: Preparation & Properties |
 73%
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Consider the following sequential reaction:
\(\begin{aligned} &\mathrm{RCH}=\mathrm{CH}_2 \xrightarrow[\mathrm{Zn} / \mathrm{H}_2 \mathrm{O}]{\mathrm{O}_3}(\mathrm{~A}) \xrightarrow{\mathrm{LAH}}(\mathrm{~B})+\text { (C), }\\ &\text { (B) and (C) are: } \end{aligned}\)
 

1.  RCHO and HCHO

2.  RCOOH and HCOOH

3. \(\mathrm{RCH}_3 \mathrm{OH} \text { and } \mathrm{HCOOH}\)

4.  

Subtopic:  Aldehydes & Ketones: Preparation & Properties |
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CH3NO23Cl2+3NaOHP.'P'is

1. CCl3CHO

2. CCl3NO2

3. CHCl3

4. CHCl2NO2

Subtopic:  Isomers & Reaction Mechanism |
 63%
Level 2: 60%+
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