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प्रश्न
Aldehydes and ketones react with hydroxylamine to form ______.
पर्याय
hydrazones
semicarbazones
cyanohydrins
oxime
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उत्तर
Aldehydes and ketones react with hydroxylamine to form oxime.
Explanation:
When aldehydes and ketones react with hydroxylamine, they undergo nucleophilic addition and create oximes.
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संबंधित प्रश्न
Write the products formed when CH3CHO reacts with the following reagents : HCN
Write the products formed when CH3CHO reacts with the following reagents : H2N – OH
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Hemiacetal
Predict the products formed when cyclohexanecarbaldehyde reacts with the following reagents.
PhMgBr and then H3O+
Reaction of aqueous sodium hydroxide on chlorobenzene gives which of the following products?
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) | ![]() |
Draw the structure of the following derivative.
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Draw structure of the following derivative.
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Draw structure of the following derivative.
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