हिंदी

How Are the Following Compounds Prepared? Acetophenone from Benzene

Advertisements
Advertisements

प्रश्न

How are the following compounds prepared?

acetophenone from benzene

Advertisements

उत्तर

(b)Acetophenone from benzene

Friedal craft reaction

shaalaa.com
  क्या इस प्रश्न या उत्तर में कोई त्रुटि है?
2012-2013 (March)

APPEARS IN

वीडियो ट्यूटोरियलVIEW ALL [1]

संबंधित प्रश्न

Write balanced chemical equations for action of ammonia on - formaldehyde


How are the following compounds prepared?

benzaldehyde from benzene


Arrange the following compound in increasing order of its reactivity in nucleophilic addition reactions.

Ethanal, Propanal, Propanone, Butanone.

Hint: Consider steric effect and electronic effect.


Predict the product of the following reaction:


Predict the product of the following reaction:


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

Imine


Predict the products formed when cyclohexanecarbaldehyde reacts with the following reagents.

PhMgBr and then H3O+


Give plausible explanation for the following:

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


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


How are the following compounds prepared?

benzaldehyde from benzoyl chloride


Write balanced chemical equations for action of ammonia on - acetone


How will you convert sodium acetate to methane?


 Acetone, Acetaldehyde, Benzaldehyde, Acetophenone – reactivity towards addition of HCN. 


Alkenes   and carbonyl compounds , both contain a π bond but alkenes show electrophilic addition reactions whereas carbonyl compounds show nucleophilic addition reactions. Explain.


Carboxylic acids contain carbonyl group but do not show the nucleophilic addition reaction like aldehydes or ketones. Why?


Which one of the following gives only one monochloro derivative?


A Idol condensation will not be observed in


Paraldehyde is formed as a result of polymerisation:-


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


What happens when ethanal is treated with excess ethanol and acid?


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)

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 structures of the following derivatives.

Acetaldehydedimethylacetal


Draw structure of the following derivative:

Acetaldehydedimethylacetal


Draw structure of the following derivative.

The ethylene ketal of hexan-3-one 


Share
Notifications

Englishहिंदीमराठी


      Forgot password?
Use app×