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

Predict the product of the following reaction: O + HO—NH2 ->[H+] - Chemistry

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प्रश्न

Predict the product of the following reaction:

रासायनिक समीकरणे/रचना

उत्तर

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पाठ 12: Aldehydes, Ketones and Carboxylic Acids - Intext Questions [पृष्ठ ३६५]

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एनसीईआरटी Chemistry [English] Class 12
पाठ 12 Aldehydes, Ketones and Carboxylic Acids
Intext Questions | Q 5.1 | पृष्ठ ३६५

संबंधित प्रश्‍न

Arrange the following in the increasing order of their reactivity towards nucleophilic addition reaction:

C6H5COCH3, CH3-CHO, CH3COCH3


Write the products formed when CH3CHO reacts with the following reagents : HCN

 


Predict the product of the following reaction:


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

Oxime


Arrange the following compounds in increasing order of their property as indicated:

Acetaldehyde, Acetone, Di-tert-butyl ketone, Methyl tert-butyl ketone (reactivity towards HCN)


Give plausible explanation for the following:

Cyclohexanone forms cyanohydrin in good yield but 2, 2, 6 trimethylcyclohexanone does not.


Explain the mechanism of alkaline hydrolysis of tert-butyl bromide with energy profile diagram.


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


Reaction of aqueous sodium hydroxide on chlorobenzene gives which of the following products?


Acetaldehyde and acetone differ in their reaction with


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

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

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)

Aldehydes and ketones react with hydroxylamine to form ______.


Draw structures of the given derivatives.

The ethylene ketal of hexan-3-one


Draw structure of the following derivative.

The ethylene ketal of hexan-3-one


Draw structure of the following derivative.

The ethylene ketal of hexan-3-one


Draw structure of the following derivative.

The ethylene ketal of hexan-3-one


Give an example of the reaction in the following case.

Oxime


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