The product 'X' in the below mentioned reaction is:

1.  2.
3. 4.

Subtopic:  Aldehydes & Ketones: Preparation & Properties |
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In the following reaction, product 'P' is:

  

1. RCOOH

2. RCHO

3. RCH3

4. RCH2OH

Subtopic:  Name Reaction |
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Match the reaction given in Column I with the corresponding name of the reaction given in Column II.

Column-I Column-II
(a) C6H5CHO + NaOH ⟶ C6H5COOH + C6H5CH2OH (i) Rosenmund reduction 
(b) \(\small(C_{6}H_{6} \ + \ CH_{3}Cl \ \xrightarrow[]{Anhyd.AlCl_{3}} C_{6}H_{5}CH_{3}\) (ii) Kolbe's reaction 
(c) \(\mathrm{RCOCl}+\mathrm{H}_2 \ \xrightarrow[]{Pd/BaSO_{4}} \ \text { RCHO }\) (iii) Claisen reaction 
(d) C6H5OH + NaOH + CO2 \(\xrightarrow[2. \ H^{+}]{1. \ Heat}\) Salicylic acid (iv) Cannizzaro reaction 
(v) Friedel-Craft's reaction 

The correct match is:

Options: (a) (b) (c) (d)
1. iv v i ii
2. v i ii iii
3. v iii ii i
4. iv ii iii i-
Subtopic:  Name Reaction |
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The most reactive compound among the following toward nucleophilic addition reaction is:

1. 2.
3. 4.
Subtopic:  Isomers & Reaction Mechanism |
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In the above reaction, the structure of ‘A’ and the type of isomerism shown in the final product are, respectively,: 

1. Prop-1-en-2-ol and Metamerism
2. Prop-1-en-1-ol and Tautomerism
3. Prop-2-en-2-ol and Geometrical isomerism
4. Prop-1-en-2-ol and Tautomerism

Subtopic:  Aldehydes & Ketones: Preparation & Properties |
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Match the acids given in Column I with their correct IUPAC names given in Column II and mark the appropriate option.

Column I
(Acids)
Column I
(IUPAC names)
(i) Phthalic acid (a) Hexane-1,6-dioic acid
(ii) Oxalic acid (b) Benzene-1,2-dicarboxylic acid
(iii) Succinic acid (c) Pentane-1,5-dioic acid
(iv) Adipic acid (d) Butane-1,4-dioic acid
(v) Glutaric acid (e) Ethane-1,2-dioic acid
 

1. (i) — (a), (ii) — (b), (iii) — (c), (iv) — (d), (v) — (e)

2. (i) — (b), (ii) — (e), (iii) — (d), (iv) — (a), (v) — (c)

3. (i) — (b), (ii) — (a), (iii) — (d), (iv) — (e), (v) — (c)

4. (i) — (a), (ii) — (e), (iii) — (c), (iv) — (b), (v) — (d)

Subtopic:  Carboxylic Acids: Preparation & Properties |
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In a set of reactions, m-bromobenzoic acid gave a product D. The product D is:

1. 2.
3. 4.
Subtopic:  Isomers & Reaction Mechanism |
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An acid that forms an anhydride (X) on heating and an acid imide (Y) on strong heating with ammonia is:

1.    2.
3. 4.   
Subtopic:  Carboxylic Acids: Preparation & Properties |
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The reactant 'A' in the below-mentioned reaction is:
 

1. Benzoyl chloride 2. Toluene
3. Acetophenone 4. Benzoic acid
Subtopic:  Acid Derivatives - Preparation, Properties & Uses |
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The major product in the following reaction is: 

1. 2.
3. 4.


 

Subtopic:  Acid Derivatives - Preparation, Properties & Uses |
 54%
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