मराठी
कर्नाटक बोर्ड पी.यू.सी.पीयूसी विज्ञान 2nd PUC Class 12

Give plausible explanation for the following: There are two −NH2 groups in semicarbazide. However, only one is involved in the formation of semicarbazones.

Advertisements
Advertisements

प्रश्न

Give plausible explanation for the following:

There are two −NH2 groups in semicarbazide. However, only one is involved in the formation of semicarbazones.

रासायनिक समीकरणे/रचना
कारण सांगा
Advertisements

उत्तर

Semicarbazide only has one of the two −NH2 groups resonance and this group is directly attached to the carbonyl-carbon atom.

Therefore, the electron density on −NH2 group involved in the resonance also decreases. As a result, it cannot act as a nucleophile. Since the other −NH2 group is not involved in resonance, it can act as a nucleophile and attack carbonyl-carbon atoms of aldehydes and ketones to produce semicarbazones.

shaalaa.com
  या प्रश्नात किंवा उत्तरात काही त्रुटी आहे का?
पाठ 8: Aldehydes, Ketones and Carboxylic Acids - Exercises [पृष्ठ २५७]

APPEARS IN

एनसीईआरटी Chemistry Part 1 and 2 [English] Class 12
पाठ 8 Aldehydes, Ketones and Carboxylic Acids
Exercises | Q 8.18 (ii) | पृष्ठ २५७

संबंधित प्रश्‍न

Write the structures of the main products when acetone (CH3 − CO − CH3) reacts with the following reagent :

H2N − NHCONH2/H+


Predict the product of the following reaction:


What is meant by the following term? Give an example of the reaction in the following case.

Schiff’s base


Write the structure of Phenylmethanamine.


Write the main product formed when propanal reacts with the following reagents: 
2 moles of 3 CH OH in presence of dry HCl 


Benzaldehyde can be obtained from benzal chloride. Write reactions for obtaining benzalchloride and then benzaldehyde from it.


Identify the compounds A, B and C in the following reaction.

\[\ce{CH3 - Br ->[Mg/ether] (A) ->[(i) CO][(ii) Water] (B) ->[CH3OH/H+][Δ] (C)}\]


The pH of blood does not appreciably change by a small addition of acid or base because


Acetaldehyde and acetone differ in their reaction with


The most stable reagent for the conversion of R – CH2OH → RCHO is


The product "P" in the above reaction is:


The increasing order of the following compounds towards HCN addition is:

(i)
(ii)
(iii)
(iv)

The product of following reaction is

\[\ce{CH3 - CH = CH - CH2 - CHO ->[i) LiAlH4][ii) H3O+]}\] ______?


Draw structures of the given derivatives.

The ethylene ketal of hexan-3-one


Draw the structure of the following derivative.

The ethylene ketal of hexane-3-one


Draw structure of the following derivative.

Acetaldehydedimethylacetal


Draw the structure of the following derivative.

Acetaldehydedimethylacetal


Draw structure of the following derivative:

Acetaldehydedimethylacetal


Draw structures of the following derivatives.

Acetaldehydedimethylacetal


Share
Notifications

Englishहिंदीमराठी


      Forgot password?
Use app×