English
Karnataka Board PUCPUC Science 2nd PUC Class 12

Why can aryl halides not be prepared by reaction of phenol with HCl in the presence of ZnClX2?

Advertisements
Advertisements

Question

Why can aryl halides not be prepared by reaction of phenol with \[\ce{HCl}\] in the presence of \[\ce{ZnCl2}\]?

Short/Brief Note
Advertisements

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.

shaalaa.com
  Is there an error in this question or solution?
Chapter 10: Haloalkanes and Haloarenes - Exercises [Page 144]

APPEARS IN

NCERT Exemplar Chemistry Exemplar [English] Class 12
Chapter 10 Haloalkanes and Haloarenes
Exercises | Q III. 63. | Page 144

RELATED QUESTIONS

Draw the structure of the major monohalo product in the following reaction:


Draw the structure of the major monohalo product in the following reaction:


Name the following halide according to the IUPAC system and classify it as an alkyl, allyl, benzyl (primary, secondary, tertiary), vinyl or aryl halide:

CH3CH = C(Cl)CH2CH(CH3)2


Name the following halide according to the IUPAC system and classify it as an alkyl, allyl, benzyl (primary, secondary, tertiary), vinyl or aryl halide:

p-ClC6H4CH2CH(CH3)2


Name the following halide according to the IUPAC system and classify it as an alkyl, allyl, benzyl (primary, secondary, tertiary), vinyl or aryl halide:

o-Br-C6H4CH(CH3)CH2CH3


Draw the structure of major monohalo product in each of the following reactions :


When two halogen atoms are attached to the same carbon atom then it is:


In which of the following molecules carbon atom marked with asterisk (*) is asymmetric?

(a) \[\begin{array}{cc}
\ce{H}\\
|\\
\phantom{.}\ce{C^*}\phantom{}\\
\phantom{}/\phantom{..}|\phantom{..}\backslash\phantom{}\\
\phantom{.}\ce{I}\phantom{...}\ce{Br}\phantom{..}\ce{Cl}
\end{array}\]

(b) \[\begin{array}{cc}
\ce{D}\\
|\\
\phantom{.}\ce{C^*}\phantom{}\\
\phantom{}/\phantom{..}|\phantom{..}\backslash\phantom{}\\
\phantom{.}\ce{I}\phantom{...}\ce{Br}\phantom{..}\ce{Cl}
\end{array}\]

(c) \[\begin{array}{cc}
\ce{H}\\
|\\
\phantom{.}\ce{C^*}\phantom{}\\
\phantom{}/\phantom{..}|\phantom{..}\backslash\phantom{}\\
\phantom{..}\ce{OH}\phantom{..}\ce{C2H5}\phantom{}\ce{CH3}
\end{array}\]

(d) \[\begin{array}{cc}
\ce{H}\\
|\\
\phantom{.}\ce{C^*}\phantom{}\\
\phantom{}/\phantom{..}|\phantom{..}\backslash\phantom{}\\
\phantom{..}\ce{H}\phantom{...}\ce{C2H5}\phantom{}\ce{CH3}
\end{array}\]


The position of \[\ce{-Br}\] in the compound in \[\ce{CH3CH = CH(Br)(CH3)2}\] can be classified as ______.


Classify the following compound as a primary, secondary and tertiary halide.

2-Bromo-2-methylpropane


Which alkyl halide has maximum density


Two isomers (A) and (B) with molar mass 184 g/mol and elemental composition C 52.2%; H 4.9% and Br 42.9% gave benzoic acid and p-bromobenzoic acid, respectively on oxidation with KMnO4. Isomer ‘A’ is optically active and gives a pale yellow precipitate when warmed with alcoholic AgNO3. Isomer ‘A’ and ‘B’ are, respectively:


Name the following halide according to IUPAC system and classify it as alkyl, allyl, benzyl (primary, secondary, tertiary), vinyl or aryl halide:

\[\ce{CH2CH2C(CH3)2CH2I}\]


Write the structure of the following organic halogen compound.

1,4-Dibromobut-2-ene


Name the following halide according to the IUPAC system and classify it as alkyl, allyl, benzyl (primary, secondary, tertiary), vinyl or aryl halide:

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 halide:

\[\ce{CH3C(CI)(C2H5)CH2CH3}\]


Name the following halide according to IUPAC system and classify as alkyl, allyl, benzyl (primary, secondary, tertiary), vinyl or aryl halides:

\[\ce{CH3C(C2H5)2CH2Br}\]


Write the structure of the following organic halogen compound.

4-tert-Butyl-3-iodoheptane


What should be the correct IUPAC name for diethylbromomethane?


Share
Notifications

Englishहिंदीमराठी


      Forgot password?
Use app×