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प्रश्न
Write balanced chemical equations for action of ammonia on - formaldehyde
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उत्तर
a. 6HCHO + 4NH3 → (CH2)6N4 + 6H2O
Formaldehyde Urotropine
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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
What is meant by the following term? Give an example of the reaction in the following case.
Acetal
What is meant by the following term? Give an example of the reaction in the following case.
Schiff’s base
Predict the products formed when cyclohexanecarbaldehyde reacts with the following reagents.
Excess ethanol and acid
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.
What are amines?
Give a simple chemical test to distinguish between 
Reaction of aqueous sodium hydroxide on chlorobenzene gives which of the following products?
Write the name of product formed, when acetone is treated with 2, 4-dinitrophenyl hydrazine.
What happens when ethanal is treated with excess ethanol and acid?
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
\[\ce{CH3 - CH = CH - CH2 - CHO ->[i) LiAlH4][ii) H3O+]}\] ______?
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 ______.
Out of p-tolualdehyde and p-nitrobenzaldehyde, which one is more reactive towards nucleophilic addition reactions, why?
Why dissociation of HCN is suppressed by the addition of HCL?
Draw structure of the following derivative.
The ethylene ketal of hexan-3-one
Draw structures of the following derivative.
The ethylene ketal of hexan-3-one
Draw the 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
The major product of the following reaction is:
