Which Of The Following Is The Most Stable Carbocation . It is a tertiary carbocation. Previous question next question >> view answer?
13 Which of the following is the most stable carbocation from galerisastro.github.io
The most stable carbocation amongst the following is answer. Therefore the tertiary carbocation having three methyl groups showing +i effect is most stable. A carbocation is a molecule in which a carbon atom has a positive charge and three bonds.
13 Which of the following is the most stable carbocation
An increased + i effect by three methyl groups stabilizes the carbocation. When a carbon atom carrying a positive charge is attached to only one alkyl group it is known as a primary carbocation. An increased + i effect by three methyl groups stabilizes the carbocation. So more the number of electron releasing groups, more is the stability.
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It is a tertiary carbocation. Asked dec 25, 2018 in principals of organic chemistry by monuk (68.1k points) organic chemistry; Therefore the tertiary carbocation having three methyl groups showing +i effect is most stable. Which of the following is the most stable carbocation (carbonium ion) ? The most stable carbocation among the following is.
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To keep reading this solution, download the app All carbocations are very reactive , so their relative reactivity doesn't matter much for the rate of a reaction. ( c h 3) 3 c +. Nothing beats the stability of aromatic cations like cyclopropenium and cycloheptatrienylium (tropylium) cations. So more the number of electron releasing groups, more is the stability.
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The positively charged carbon atom is bonded with two carbon atoms and one hydrogen atom, so we will call it a secondary carbocation and it will be less stable than tertiary carbocation. Carbocation it o carbocation iii carbocation ii and iii are equivalently stable. Will be the most stable carbocation amongst the other carbocations given. The order of stability is.
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Will be the most stable carbocation amongst the other carbocations given. Which one of the following carbocations, as drawn, is the most stable? When a carbon atom carrying a positive charge is attached to only one alkyl group it is known as a primary carbocation. Greater is the number of alkyl groups attached to c atom bearing positive charge, greater.
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Carbocation is more stable if it is bonded to electron relasing group which somewhat stabilise the carbocation. Hence the most stable carbocation is tertiary. Which of the following is the most stable carbocation (carbonium ion)? The positively charged carbon atom is bonded with two carbon atoms and one hydrogen atom, so we will call it a secondary carbocation and it.
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Asked dec 25, 2018 in principals of organic chemistry by monuk (68.1k points) organic chemistry; The most stable carbonium ion among the following is. Hence, the most stable carbocation is triphenyl methyl carbocation. Add the conjugation with cyclopropyl rings, and the most stable carbocation prepared to date is probably the tricyclopropylcyclopropenium cation. Important points greater the number of resonating structures,.
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This stability order is described with the help of hyperconjugation and inductive effect. The order of carbocation stability is t e r t i a r y > s e c o n d a r y > p r i m a r y > m e t h y l. 19 related question answers found − n o.
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( c h 3) 3 c +. See the answer see the answer see the answer done loading. Tertiary carbocation is the most stable due to hyperconjugation effect followed by secondary carbocation and then primary carbocation. Thus, the correct option is (b). Which of the following is the most stable carbocation?
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Will be the most stable carbocation amongst the other carbocations given. The order of stability of carbocation is `benzyl cation gt 3^(@) cation gt 2^(@) cation gt 1^(@) cation` `c_(6)h_(5)overset(o+)ch_(2)`, a benzyle cation, is thr most stable due to resonance stabilization. This problem has been solved! So more the number of electron releasing groups, more is the stability. The positively.
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A tertiary carbocation is the most stable carbocation due to the electron releasing effect of three methyl groups. So, we can say that. − n o 2 group exhibit − i effect and it decreases with increase in distance. An increased + i effect by three methyl groups stabilizes the carbocation. Add the conjugation with cyclopropyl rings, and the most.
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Nothing beats the stability of aromatic cations like cyclopropenium and cycloheptatrienylium (tropylium) cations. A tertiary carbocation is the most stable carbocation due to the electron releasing effect of three methyl groups. Which of the following is the most stable carbocation (carbonium ion)? The most stable carbocation among the following is. It is a tertiary carbocation.
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On the basis of hyper conjugation, ( c h 3) 2 c + h shows six resonating structures. So, we can say that. Some basic principles and techniques; Therefore the tertiary carbocation having three methyl groups showing +i effect is most stable. The most stable carbocation among the following is.
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The order of carbocation stability is t e r t i a r y > s e c o n d a r y > p r i m a r y > m e t h y l. The most stable carbocation among the following is. Carbocation is more stable if it is bonded to electron relasing group which.
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The most stable carbonium ion among the following is. C h 3 − c h 3 ∣ c + ∣ c h 3 is the most stable carbocation. This stability order is described with the help of hyperconjugation and inductive effect. See the answer see the answer see the answer done loading. The most stable carbocation is :
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Thus, carbocation (b) has the highest number of methyl groups and so it is the most stable carbocation. All carbocations are very reactive , so their relative reactivity doesn't matter much for the rate of a reaction. Add the conjugation with cyclopropyl rings, and the most stable carbocation prepared to date is probably the tricyclopropylcyclopropenium cation. ( c h 3).
