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Name the electrophile produced in the reaction of benzene with benzoyl chloride in the presence of anhydrous AlClX3. Name the reaction also. - Chemistry

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प्रश्न

Name the electrophile produced in the reaction of benzene with benzoyl chloride in the presence of anhydrous \[\ce{AlCl3}\]. Name the reaction also.

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उत्तर

\[\begin{array}{cc}
\phantom{}\ce{O}\phantom{.......................}\ce{O}\phantom{...............................}\\
\phantom{}||\phantom{.......................}||\phantom{...............................}\\
\ce{C6HC - Cl + AlCl3 -> C6H5\overset{δ+}{C - Cl} = \overset{δ-}{Alcl3} -> C6H5Co+ + AlCl4}
\end{array}\]

Friedel–Crafts acylation reaction.

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अध्याय 12: Aldehydes, Ketones and Carboxylic Acids - Multiple Choice Questions (Type - I) [पृष्ठ १७३]

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एनसीईआरटी एक्झांप्लर Chemistry [English] Class 12
अध्याय 12 Aldehydes, Ketones and Carboxylic Acids
Multiple Choice Questions (Type - I) | Q 25 | पृष्ठ १७३

संबंधित प्रश्न

How will you bring about the following conversion?

Benzoyl chloride to benzaldehyde.


How will you prepare the given compound from benzene? You may use any inorganic reagent and any organic reagent having not more than one carbon atom.

p-Nitrobenzaldehyde


When 0.4 g of acetic acid is dissolved in 40 g of benzene, the freezing point of the solution is lowered by 0.45 K. Calculate the degree of association of acetic acid. Acetic acid forms dimer when dissolved in benzene.
(Kf for benzene = 5.12 K kg mol−1, at. wt. C = 12, H = 1, O = 16)


Ozonolysis of alkenes followed by the reaction with zinc dust and water gives ____________ depending on the substitution pattern of the alkene.


The oxidation of toluene to benzoic acid can be stopped at the aldehyde stage to give benzaldehyde. The reagent used for the purpose is one of the following.


Match the common names given in Column I with the IUPAC names given in Column II.

  Column I
(Common names)
  Column II
(IUPAC names)
(i) Cinnamaldehyde (a) Pentanal
(ii) Acetophenone (b) Prop-2-enal
(iii) Valeraldehyde (c) 4-Methylpent-3-en-2-one
(iv) Acrolein (d) 3-Phenylprop-2-enal
(v) Mesityl oxide (e) 1-Phenylethanone

Match the example given in Column I with the name of the reaction in Column II.

  Column I
(Example)
  Column II
(Reaction)
(i) \[\begin{array}{cc}
\phantom{...}\ce{O}\phantom{..............................}\ce{O}\phantom{}\\
\phantom{...}||\phantom{..............................}||\phantom{}\\
\ce{CH3 - C - Cl + H2 ->[Pd - C/BasO4] CH3 - C - H}
\end{array}\]
(a) Friedel Crafts acylation
(ii) (b) HVZ reaction
(iii) (c) Aldol condensation
(iv) \[\begin{array}{cc}
\ce{R - CH2 - COOH ->[Br/Red P] R - CH - COOH}\\
\phantom{.....................}|\\
\phantom{.......................}\ce{Br}
\end{array}\]
(d) Cannizaro’s reaction
(v) \[\ce{CH3 - CN ->[(i) SnCl2/HCl][(ii) H2O/H+] CH3CHO}\] (e) Rosenmund’s reductio
(vi) \[\ce{2CH3CHO ->[NaOH] CH3 - CH = CHCHO}\] (f) Stephen’s reaction

An alkene ‘A’ (Mol. formula \[\ce{C5H10}\]) on ozonolysis gives a mixture of two compounds ‘B’ and ‘C’. Compound ‘B’ gives positive Fehling’s test and also forms iodoform on treatment with \[\ce{I2}\] and \[\ce{NaOH}\]. Compound ‘C’ does not give Fehling’s test but forms iodoform. Identify the compounds A, B and C. Write the reaction for ozonolysis and formation of iodoform from B and C.


What is the name of the given reaction of preparation of aldehyde?

\[\ce{C3COCl ->[H2][Pd/BaSO4] CH3CHO + HCl}\]


\[\begin{array}{cc}
\ce{CH3 - CH2 - CH - CH3}\\
\phantom{.....}|\\
\phantom{......}\ce{Cl}
\end{array}\]  obtained by chlorination of n-butane, will be


The number of chiral carbon in glucose is:-


Aldehydes are the first oxidation products of ______.


Predict the reagent for carrying out the following transformations:

Benzoyl chloride to Benzaldehyde


Reagent used to convert allyl alcohol to acrolein is ______.


Account for the following:

N-ethylbenzene sulphonyl amide is soluble in alkali.


Account for the following:

Reduction of nitrobenzene using Fe and HCl is preferred over Sn and HCl.


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