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Why CH(3)Cl is easily hydrolysed than C(...

Why `CH_(3)Cl` is easily hydrolysed than `C_(6)H_(5)Cl`?

Answer

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CH_(3)CI undergoes hydrolysis more easily than C_(6)H_(5)CI . Explain.

Out of C_(6)H_(5)CH_(2)CL and C_(6)H_(5)CHCIC_(6)H_(5) , which is more easily hydrolysed by aqueous KOH?

Knowledge Check

  • The main reason that SiCl_4 is easily hydrolysed as compared to C Cl_4 is that -

    A
    Si-Cl bond is weaker than C-Cl bond
    B
    `SiCl_4` can form hydrogen bonds
    C
    `SiCl_4` is covalent
    D
    Si can extend its coordination number beyond four

  • SiCl_4 gets readily hydrolysed but C Cl_4 does not, because-

    A
    Si can expand its octet but C does not
    B
    ionisation enthalpy of C is greater than that of Si
    C
    C forms both double and triple bonds
    D
    electronegativity of C is greater than that of Si

    • Similar Questions

    Explore conceptually related problems

    CH_(3)CI undergoes hydrolysis much easily as compared to C_(6)H_(5)CI . Explain with reasons.

    Explain why CH_(3)Cl undergoes hydrolysis at a faster rate in the presence of Nal.

    Assertion: Cleavage of anisole with HBr at 373 K gives phenol and CH_(3)Br Reason : Due to resonance, O-C_(6)H_(5) bond is stronger than O-CH_(3) bond.

    The dipole moment of CH_(3)F is less than that of CH_(3)Cl , though F is more electronegative than Cl-explain.

    Which one of each pair undergoes S_(N)I reaction readily and why? (ii) CH_(3)0CH_(2)Cl, CH_(3)OCH_(2)CH_(2)Cl .

    Which one of each pair of compounds will undergo S_(N)1 reaction readily and why? (ii) CH_(3)OCH_(2)Cl, CH_(3)OCH_(2)CH_(2)Cl .

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