Advertisements
Advertisements
Question
Why can aryl halides not be prepared by reaction of phenol with \[\ce{HCl}\] in the presence of \[\ce{ZnCl2}\]?
Solution
Aryl halides can't be prepared by reaction of phenol with \[\ce{HCl}\] in presence of \[\ce{ZnCl2}\] because the carbon-oxygen bond in phenols has partial double bond character and it, being stronger than a single bond, is difficult to break.
APPEARS IN
RELATED QUESTIONS
Name the following halide according to the IUPAC system and classify it as an alkyl, allyl, benzoyl (primary, secondary, tertiary), vinyl or aryl halide:
CH3CH(CH3)CH(Br)CH3
m-Xylene reacts with Br2 in presence of FeBr3, what are products formed:
Which of the following is an example of vic-dihalide?
Which alkyl halide has maximum density
Classify the following compound as a primary, secondary and tertiary halide.
1-Bromobut-2-ene
Which of the following belongs to the class of vinyl halides?
Name the following halide according to IUPAC system and classify them as alkyl, allyl, benzyl (primary, secondary, tertiary), vinyl or aryl halides:
\[\ce{CH3C(Cl)(C2H5)CH2CH3}\]
Name the following halide according to IUPAC system and classify them as alkyl, allyl, benzyl (primary, secondary, tertiary), vinyl or aryl halides:
\[\ce{CH3 CH2 C(CH3)2 CH2I}\]
Name the following halide according to IUPAC system and classify as alkyl, allyl, benzyl (primary, secondary, tertiary), vinyl or aryl halides:
\[\ce{CH3C(C2H5)2CH2Br}\]
Name the following halides according to IUPAC system and classify them as alkyl, allyl, benzyl (primary, secondary, tertiary), vinyl or aryl halides:
\[\ce{CH3CH2C(CH3)2CH2I}\]