Advertisements
Advertisements
प्रश्न
What is meant by the following term? Give an example of the reaction in the following case.
2, 4-DNP-derivative
Advertisements
उत्तर
When an aldehyde or ketone reacts with 2, 4-dinitrophenylhydrazine in a weak acidic medium, 2, 4-dinitrophenylhydrazone (2, 4-DNP derivative) is produced.

APPEARS IN
संबंधित प्रश्न
Acetaldehyde, when treated with which among the following reagents does NOT undergo addition reaction?
(A) Ammonia
(B) Hydroxylamine
(C) Ammoniacal silver nitrate
(D) Semicarbazide
Write the structures of the main products when acetone (CH3 − CO − CH3) reacts with the following reagent :
H2N − NHCONH2/H+
Write the products formed when CH3CHO reacts with the following reagents : HCN
Predict the product of the following reaction:

Predict the product of the following reaction:

How will you bring about the following conversion in not more than two steps?
Bromobenzene to 1-Phenylethanol
Explain the mechanism of alkaline hydrolysis of tert-butyl bromide with energy profile diagram.
How are the following compounds prepared?
benzaldehyde from benzoyl chloride
Write balanced chemical equations for action of ammonia on - acetaldehyde
Write balanced chemical equations for action of ammonia on - acetone
Write balanced chemical equations for action of ammonia on - acetone
Reaction of aqueous sodium hydroxide on chlorobenzene gives which of the following products?
Which one of the following gives only one monochloro derivative?
Which will undergo faster nucleophilic addition reaction?
Acetaldehyde or Propanone

The product "P" in the above reaction is:
The following questions are case-based questions. Read the passage carefully and answer the questions that follow:
| The carbon-oxygen double bond is polarised in aldehydes and ketones due to higher electronegativity of oxygen relative to carbon. Therefore, they undergo nucleophilic addition reactions with a number of nucleophiles such as HCN, NaHSO3, alcohols, ammonia derivatives and Grignard reagents. Aldehydes are easily oxidised by mild oxidising agents as compared to ketones. The carbonyl group of carboxylic acid does not give reactions of aldehydes and ketones. Carboxylic acids are considerably more acidic than alcohols and most of simple phenols. |
Answer the following:
(a) Write the name of the product when an aldehyde reacts with excess alcohol in the presence of dry HCl. (1)
(b) Why carboxylic acid is a stronger acid than phenol? (1)
(c) (i) Arrange the following compounds in increasing order of their reactivity towards CH3MgBr: (1)
CH3CHO, \[\begin{array}{cc}
\ce{(CH3)3C-C-CH3}\\
\phantom{....}||\\
\phantom{....}\ce{O}
\end{array}\], \[\begin{array}{cc}
\ce{CH3-C-CH3}\\
||\\
\ce{O}
\end{array}\]
(ii) Write a chemical test to distinguish between propanal and propanone. (1)
OR
(c) Write the main product in the following: (2)
| (i) | ![]() |
| (ii) | ![]() |
Draw the structure of the following derivative.
The ethylene ketal of hexane-3-one
Draw structure of the following derivative.
The ethylene ketal of hexan-3-one
Draw structures of the following derivatives.
Acetaldehydedimethylacetal
Draw structures of the given derivatives.
The ethylene ketal of hexan-3-one


