Determine the decreasing order of stability for the following carbocations: $(I) \ CH_3-C^+(CH_3)-CH_3$,$(II) \ CH_3-CH^+(OCH_3)$,$(III) \ CH_3-CH^+(COCH_3)$.

  • A
    $I > II > III$
  • B
    $III > II > I$
  • C
    $II > III > I$
  • D
    $II > I > III$

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Similar Questions

Choose the most reasonable reaction intermediate for the following reaction.

Assertion : Carbanions like ammonia have pyramidal shape.
Reason : The carbon atom carrying negative charge has an octet of electrons.

The decreasing order of hydride affinity for the following carbocations is:
$A: CH_2=CH-C^+(CH_3)_2$
$B: (C_6H_5)_3C^+$
$C: (CH_3)_3C^+$
$D: (Cyclopropyl)_3C^+$
Choose the correct answer from the options given below:

Which one of the following carbocations is the most stable?

The stability of carbanions follows the order:
$I: CH_3CH_2CH_2\bar{C}H_2$
$II: CH_3\bar{C}HCH_2CH_3$
$III: (CH_3)_3\bar{C}$
$IV: CH_3\bar{C}(Ph)CH_2CH_3$

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