Advertisements
Advertisements
प्रश्न
How are the following compounds prepared?
acetophenone from benzene
Advertisements
उत्तर
(b)Acetophenone from benzene

Friedal craft reaction
APPEARS IN
संबंधित प्रश्न
Draw the structure of the semicarbazone of ethanal.
Write the products formed when CH3CHO reacts with the following reagents : HCN
Predict the product of the following reaction:
\[\begin{array}{cc}
\phantom{..............}\ce{O}\\
\phantom{..............}||\\
\ce{R - CH = CH - CHO + NH2 - C - NH - NH2 ->[H+]}\end{array}\]
Predict the products formed when cyclohexanecarbaldehyde reacts with the following reagents.
Semicarbazide and weak acid
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
Complete the synthesis by giving missing starting material, reagent or product.

Explain the mechanism of alkaline hydrolysis of tert-butyl bromide with energy profile diagram.
Write balanced chemical equations for action of ammonia on - acetone
Write the structure of Phenylmethanamine.
Give a simple chemical test to distinguish between
Write the main product formed when propanal reacts with the following reagents:
2 moles of 3 CH OH in presence of dry HCl
Write a test to differentiate between pentan-2-one and pentan-3-one.
Benzaldehyde can be obtained from benzal chloride. Write reactions for obtaining benzalchloride and then benzaldehyde from it.
Carboxylic acids contain carbonyl group but do not show the nucleophilic addition reaction like aldehydes or ketones. Why?
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
Which of the following has the most acidic hydrogen?
Grignard reagent on reaction with acetone forms.
Arrange the following in the increasing order of their property indicated:
Ethanal, Propanone, Propanal, Butanone (reactivity towards nucleophilic addition)
The increasing order of the following compounds towards HCN addition is:
| (i) | ![]() |
| (ii) | ![]() |
| (iii) | ![]() |
| (iv) | ![]() |
In the following reaction
\[\ce{Carbonyl compound + MeOH <=>[HCl] acetal}\]
Rate of the reaction is the highest for ______.
Draw the structure of the following derivative.
The ethylene ketal of hexane-3-one
Draw structure of the following derivative.
The ethylene ketal of hexane-3-one
Why dissociation of HCN is suppressed by the addition of HCL?
Draw structure of the following derivative:
Acetaldehydedimethylacetal
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 the structure of the following derivative.
Acetaldehydedimethylacetal
Give an example of the reaction in the following case.
Oxime




