RCOOH RCH2OH. This mode of reduction of an acid to alcohol can be affected only by:

1. Zn/HCl

2. Na-alcohol

3. aluminium isopropoxide and isopropyl alcohol

4. LiAlH4

 

Subtopic:  Aldehydes & Ketones: Preparation & Properties |
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Compound (A) C5H10O forms a phenyl hydrazone and gives negative Tollen's and iodoform tests. Also, compound (A) on reduction gives n-pentane. Compound (A) is-

1. A primary alcohol 2. An aldehyde
3. A ketone 4. A secondary alcohol 
Subtopic:  Aldehydes & Ketones: Preparation & Properties |
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Formaldehyde can be distinguished from acetaldehyde by:

1. Fehling's solution                     

2. Schiff's reagent

3. Ammonia                               

4. Ammoniacal AgNO3

Subtopic:  Aldehydes & Ketones: Preparation & Properties | Name Reaction |

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What is the chemical reaction of lachrymator or tear gas?

1. C6H5COCl                               

2. C6H5OC6H5

3. C6H5COCH2Cl                         

4. C6H5COCH3

Subtopic:  Acid Derivatives - Preparation, Properties & Uses | Name Reaction |
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HCHO and HCOOH are distinguished by treating with:

1. Tollens reagent

2. NaHCO3

3. Fehling's Solution

4. Benedict Solution

Subtopic:  Aldehydes & Ketones: Preparation & Properties |
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A compound that gives two different alcohols on reduction with LiAlH4 is:

1. CH3COOCH3                         

2. CH3COOC2H5

3. CH3COCH3                           

4. CH3CHO

Subtopic:  Aldehydes & Ketones: Preparation & Properties | Isomers & Reaction Mechanism | Acid Derivatives - Preparation, Properties & Uses |
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The compound formed when malonic acid heated with urea, is-                 

1. Cinnamic acid

2. Butyric acid

3. Barbituric acid

4. Crotonic acid

Subtopic:  Acid Derivatives - Preparation, Properties & Uses |
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An ester is boiled with KOH. The product is cooled and acidified with conc. HCl. A white crystalline acid separates. The ester is-

1. Methyl acetate                       

2. Ethyl acetate

3. Ethyl formate                         

4. Ethyl benzoate

Subtopic:  Acid Derivatives - Preparation, Properties & Uses |
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 A and B in the following reactions are R-C||O-R'KCNHCN/AB

1. A=RR'CH2CN, B=NaOH

2. A=, B=CH3

3. A=, B=CH3

4. A=, B=LiAlH4

Subtopic:  Aldehydes & Ketones: Preparation & Properties |
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Consider the following transformations

CH3COOH CaCO3AheatBNaOHI2C The molecular formula of C is                       

1. CH3-C||IOH-CH3

2. ICH2-COCH3

3. CHI3

4. CH3I

 

Subtopic:  Acid Derivatives - Preparation, Properties & Uses |
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