Advertisements
Advertisements
प्रश्न
Write the structures and names of the compounds formed when compound ‘A’ with molecular formula, \[\ce{C7H8}\] is treated with \[\ce{Cl2}\] in the presence of \[\ce{FeCl3}\].
Advertisements
उत्तर
The compound with molecular formula \[\ce{C7H8}\] is toluene, \[\ce{C6H5CH3}\]. Since \[\ce{^-CH3}\] group is o-, p-directing, therefore, chlorination of toluene gives o-chlorotoluene and p-chlorotoluene, in which the p-isomer predominates.
APPEARS IN
संबंधित प्रश्न
Which would undergo SN1 reaction faster in the following pair and why?

Give reasons for the following:
(CH3)3C–O–CH3 on reaction with HI gives (CH3)3C–I and CH3–OH as the main products and not (CH3)3C–OH and CH3–I.
The stability order for carbocation is _______.
(A) 2° > 3° > 1°
(B) 3° > 2° > 1°
(C) 3° > 1° > 2°
(D) 1° > 3° > 2°
What is the action of the following on ethyl bromide
alcoholic solution of potassium hydroxide.
What is the action of the following on ethyl bromide:
moist silver oxide
What is the action of the following on ethyl bromide?
silver acetate
Most reactive halide towards SN1 reaction is ____________.
SN2 mechanism proceeds through intervention of ____________.
Which among MeX, RCH2X, R2CHX and R3CX is most reactive towards SN2 reaction?
Identify X and Y in the following sequence:
\[\ce{C2H5Br ->[X] Product ->[Y] C3H7NH2}\]
The correct order of increasing the reactivity of C–X bond towards nucleophile in following compounds.

(I)

(II)
(CH3)3CCl
(III)
(CH3)2CHCl
(IV)
Which of the following compound will undergo racemisation when reacts with aq. KOH?
(i)

(ii)
CH3CH2CH2Cl
(iii)
\[\begin{array}{cc}
\ce{CH3}\phantom{..}\\
|\phantom{....}\\
\ce{CH3-CH-CH2Cl}
\end{array}\]
(iv)
\[\begin{array}{cc}
\phantom{..}\ce{H}\\
\phantom{..}|\\
\ce{CH3-C-Cl}\\
\phantom{..}|\\
\phantom{.....}\ce{C2H5}
\end{array}\]
Which of the following statements are correct about this reaction?

(i) The given reaction follows SN2 mechanism.
(ii) (b) and (d) have opposite configuration.
(iii) (b) and (d) have same configuration.
(iv) The given reaction follows SN1 mechanism.
Ethylene chloride and ethylidene chloride are isomers. Identify the correct statements.
(i) Both the compounds form same product on treatment with alcoholic KOH.
(ii) Both the compounds form same product on treatment with aq.NaOH.
(iii) Both the compounds form same product on reduction.
(iv) Both the compounds are optically active.
Chlorination of alkanes is an example of
In which reaction mechanism carbocation is formed?
The major product formed in the following reaction is:

Explain why Grignard reagents should be prepared under anhydrous conditions.
