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Which is more stable CH3+ or Cd3+?

Which is more stable CH3+ or Cd3+?

CARBOCATION STABILITY=>postive charge species i.e. electron deficient. Hence any electron donating grp(EDG) will stabilize it . SO, Cd3+ is more stable than Ch3+… (since C-D bond has more electron density).

Is Cd3 more stable than CH3?

CARBANION STABILITY =>negatively charged species i.e. electron present in excess. Hence any electron withdrawing grp(EWG) will stabilise it. SO, Ch3- is more stable than Cd3-…

Which of carbocation is most stable?

tertiary carbocation
The carbocation bonded to three alkanes (tertiary carbocation) is the most stable, and thus the correct answer. Secondary carbocations will require more energy than tertiary, and primary carbocations will require the most energy.

Which one is the most stable carbocation a c6h5 C+ B CH3 3C+ C CH3 2hc+ D h3c+?

3° carbocation (CH₃)₃ C+ is the most stable carbocation.

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Which is more stable CH3 3C or CD3 3C?

Explanation: since hyperconjugation effect of CH3 is more than CD3.

Which of the following Carbocation is most stable CH3 ch2?

(CH3)3+C is a tertiary carbocation. A tertiary carbocation is the most stable carbocation due to the electron releasing effect of three methyl groups.

Which Carbocation is most stable CH3?

Which carbocation is least stable?

-Hence, out of the given options, the carbocation that has the least number of substituents is $C{H_3} – C{H_2} – \mathop {C{H_2}}\limits^ + $. So, it will be the least stable species.

Which carbocation is more stable CH3 C or ch3ch2c?

(CH3)3C+ i.e 3° carbocation is more stable carbocation than 1° carbocation i.e CH3+ or CH3CH2+ because 3° carbocation has more hyper conjunction effect i.e it has 9 alpha hydrogen which is more stable but CH3+ has 0 aplha hydrogen thats why it is least stable carbocation and CH3CH2+ has 3 alpha hydrogen it is also less …

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Which is more stable CH3 3C+ or CD3 3C+?

Which shows more +I effect CH3 or CD3?

Basically as the mass of isotopes increases, bond vibration decreases and thus heavier isotopes will be more closer to carbon for a longer time. So the inductive effect order is CT3>CD3>CH3, however the order get reversed in case of hyperconjugation.