In the following reaction: 

\(\text {HC} \equiv \text {CH} \xrightarrow [Hg^{2+}] { H_2SO_4} P \)

Product 'P' will not give 
1. Tollen's reagent test 
2. Fehling's solution
3. Victor Meyer test 
4. Iodoform test 

Subtopic:  Aldehydes & Ketones: Preparation & Properties |
 66%
From NCERT
NEET - 2013
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The correct order of reactivity of phenyl magnesium bromide (PhMgBr) with the following
compounds will be:

I II III

1. I > II > III 

2. III > II > I

3. II > I > III 

4. I > III > II

Subtopic:  Isomers & Reaction Mechanism |
 76%
From NCERT
AIPMT - 2011
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Match the compounds given in List-I with List-II and select the suitable option from the code given below:

List-I List-II

(a) Benzaldehyde

(i) Phenolphthalein

(b) Phthalic anhydride

(ii) Benzoin condensation

(c) Phenyl benzoate

(iii) Oil of wintergreen

(d) Methyl salicylate

(iv) Fries rearrangement

Codes:

(a) (b) (c) (d)
1. (ii) (i) (iv) (iii)
2. (iv) (i) (iii) (ii)
3. (iv) (ii) (iii) (i)
4. (ii) (iii) (iv) (i)
Subtopic:  Name Reaction |
 66%
AIPMT - 2011
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Match the compounds given in List -I with their characteristic reactions given in List -II. Select the correct option.

List – I (Compounds) List – II (Reactions)
(a) CH3CH2CH2CH2NH2 (i) Alkaline hydrolysis
(b) CH3C≡CH (ii) With KOH (alcohol) and CHCl3 produce a bad smell.
(c) CH3CH2COOCH3 (iii) Gives white ppt. with ammoniacal AgNO3
(d) CH3CH(OH)CH3 (iv) With Lucas' reagent cloudiness appears after 5 minutes.

Options :

(a) (b) (c) (d)
1. (iii) (ii) (i) (iv)
2. (ii) (iii) (i) (iv)
3. (iv) (ii) (iii) (i)
4. (ii) (i) (iv) (iii)
Subtopic:  Aldehydes & Ketones: Preparation & Properties | Carboxylic Acids: Preparation & Properties |
 76%
From NCERT
AIPMT - 2010
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Consider the following reaction:

The product 'A' is:

1. C6H5OH

2. C6H5COCH3

3. C6H5Cl

4. C6H5CHO

Subtopic:  Name Reaction |
 91%
From NCERT
AIPMT - 2012
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 A yellow precipitate with iodine and alkali is given by:

(i).  Methyl acetate

(ii).  Acetamide

(iii).  2-Hydroxypropane

(iv).  Acetophenone

1. (i), and (ii)
2. (ii), and (iii)
3. (iii), and (iv)
4. (iv), and (i)

Subtopic:  Name Reaction |
 54%
From NCERT
AIPMT - 2012
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Consider the reaction:

RCHO + NH2NH2RCH =N-NH2

What sort of reaction is it?
1.  Free radical addition – elimination reaction
2. Electrophilic substitution-elimination reaction
3.  Nucleophilic addition – elimination reaction
4.  Electrophilic addition – elimination reaction

Subtopic:  Aldehydes & Ketones: Preparation & Properties |
 74%
From NCERT
AIPMT - 2012
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The self-condensation product of two moles of ethyl acetate in the presence of sodium ethoxide yield is: 

1. Ethyl butyrate

2. Acetoacetic ester

3. Methyl acetoacetate

4. Ethyl propionate

Subtopic:  Aldehydes & Ketones: Preparation & Properties | Name Reaction |
AIPMT - 2006
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The nucleophilic addition reaction will be most favored among the given compounds is:

1. CH3CH2CH2COCH3

2. (CH3)2C=O

3. CH3CH2CHO

4. CH3CHO

Subtopic:  Isomers & Reaction Mechanism |
 70%
From NCERT
AIPMT - 2006
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A carbonyl compound reacts with hydrogen cyanide to form cyanohydrins, which form a racemic mixture of α-hydroxy acid on hydrolysis. The carbonyl compound is:

1. Acetaldehyde

2. Acetone

3. Diethyl ketone

4. Formaldehyde

Subtopic:  Aldehydes & Ketones: Preparation & Properties | Isomers & Reaction Mechanism |
 63%
From NCERT
AIPMT - 2006
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