Do halohydrins experience hydride and or methyl shifts
Do halohydrins experience hydride and or methyl shifts
Homework Answers
ANSWER:
The answer is NO. As per existing knowledge in Organic chemistry, the said hydride and methyl shifts are not possible with halohydrins.
Halohydrins do not experience either a hydride shift or methyl shift.
Hydride and methyl shifts are experienced in SN1 and E1 reaction intermediates which are basically carbocations.
These hydride and methyl shifts are thermodynamically favored only if the intermediate carbocation that is to be formed as the result of hydride or methyl shift is relatively highly branched. (i.e., if the initially formed carbocation is having a secondary C atom and if it may result in a tertiary carbocation as the result of a hydride or a methyl shift, it is favored.)
Write chemical reactions to show the different products that may result from intramolecular hydride and methyl...
Write chemical reactions to show the different products that may result from intramolecular hydride and methyl shifts (involving the end monomeric unit) in cationic polymerization of 3-methyl-1-pentene.
please explain step by step how do this problem. it is a carbocation rearrangement. (hydride/methyl shift)
please explain step by step how do this problem. it is
a carbocation rearrangement. (hydride/methyl shift)
4. Write chemical reactions to show the different products that may result from intramolecular hydride and...
4. Write chemical reactions to show the different products that may result from intramolecular hydride and methyl shifts (involving the end monomeric unit) in cationic polymerization of 3-methyl-1-pentene.
Help Review hydride shifts following reactions: (in your textbook). Propose a mechanism for each of the...
Help
Review hydride shifts following reactions: (in your textbook). Propose a mechanism for each of the following reactions:
Which of the following carbocation(s) can undergo a methyl shift OR Hydride shift to be more...
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
Show the products (major) and mechanism of 3-methyl-butene + HCl. Also, include the hydride shift
Show the products (major) and mechanism of 3-methyl-butene + HCl. Also, include the hydride shift
Which of the following carbocation(s) cannot undergo a methyl shift or a hydride shift to be...
Which of the following carbocation(s) cannot undergo a methyl shift or a hydride shift to be more stable than it was? Select one or more: a. Carbocation b b. Carbocationc c.Carbocation a d. Carbocation d
Select all of the molecules that will readily undergo a 1.2-hydride or a 1.2-methyl shift to...
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
propose a mechanism involving a hydride shift or a methyl shift for each reaction. Explain how...
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
Which of the following carbocation(s) can undergo a methyl shift OR Hydride shift to be more...
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
Write chemical reactions to show the different products that may result from intramolecular hydride and methyl shifts (involving the end monomeric unit) in cationic polymerization of 3-methyl-1-pentene.
please explain step by step how do this problem. it is
a carbocation rearrangement. (hydride/methyl shift)
4. Write chemical reactions to show the different products that may result from intramolecular hydride and methyl shifts (involving the end monomeric unit) in cationic polymerization of 3-methyl-1-pentene.
Help
Review hydride shifts following reactions: (in your textbook). Propose a mechanism for each of the following reactions:
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) cannot undergo a methyl shift or a hydride shift to be more stable than it was? Select one or more: a. Carbocation b b. Carbocationc c.Carbocation a d. Carbocation d
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
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
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
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