Ans :- Carbocation (b) and Carbocation (d) are the carbocations which do not undergoes hydride or methyl shifting.
Explanation :-
Hydride (H-) shifting or methyl shifting (CH3-) is a type of rearrangement which only occurs in order to acheive the stability of a carbocation.
The decreasing order of stability order of carbocation is :
Tertiary carbocation > Secondary carbocation > Primary carbocation.
Which of the following carbocation(s) cannot undergo a methyl shift or a hydride shift to be...
Which of the following carbocation(s) can undergo a methyl shift OR Hydride shift to be more stable than it was? o den 8 a Select one or more: a. Carbocation a b. Carbocation d B c. Carbocationc d. Carbocation b
Which of the following carbocation(s) can undergo a methyl shift OR Hydride shift to be more stable than it was? Do blood Select one or more: a. Carbocation d b. Carbocation a c. Non of the above d. Carbocationc e. Carbocation b
Which of the following carbocation(s) can undergo a methyl shift and hydride shift to be more stable than it was? Oo ngoa Select one: O a. Non of the above O b. Carbocation a o c. Carbocation b O d. Carbocationc O e. Carbocation d
which of the following carbocations can undergo a hydride shift to be more stable than it was? Which of the following carbocation(s) can undergo a hydride shift to be more stable than it was? which of the follow do y como Select one: a. Carbocationc b. none of the carbocations c. Carbocation a O d. Carbocation d e. Carbocation b
Select all of the molecules that will readily undergo a 1.2-hydride or a 1.2-methyl shift to form a more stable carbocation. 5th attempt alul See Periodic Table O Se Choose one or more: UA B. D. E OF D G BH
From the list of carbocations below, select the carbocation(s) that can rearrange via hydride shift to a more stable carbocation. CH2
please explain step by step how do this problem. it is a carbocation rearrangement. (hydride/methyl shift)
Question 9 1 pts Which ane of the following carbocations, as drawn, is the mast stable? Me CH (methyl cation) Cна Me Me Question 10 1 pts With respect to the previous question, which carbocation (A, B, C, D, or E) is most likely to undergo a 1,2-hydride shift to generate a more stable carbocation? A
Which of the following carbocations is the least stable? Do uhradar Select one: O a. carbocation b © b. carbocation d O c. carbocationc d. None of the above e. carbocation a YHLE
propose a mechanism involving a hydride shift or a methyl shift for each reaction. Explain how each rearrangement forms a more stable intermediate by using "electron-pushing". CH, I (a) CH-6-CH-CH, CHLOH