Examine the reaction/mechanism provided for the acid-catalyzed dehydration of 2-methyl-2-butanol. Select all the following statements that are correct. OH 1 H₂SO4 + H 20-1-04 -OH 2 X- OH₂ 3 + O-S-OH Ö 4 + H₂O 6 5 GA. The dehydration reaction proceeds via an E1 mechanism. B. Compound 6 is the most stable alkene formed by the dehydration. C. The curved arrows, as shown in Compound 5, result in the formation of Compound 6. D. Compound 6 is not the most stable alkene produced by the dehydration. E. The dehydration reaction proceeds via an E2 mechanism.

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Examine the reaction/mechanism provided for the acid-catalyzed dehydration of 2-methyl-2-butanol. Select all the following statements that are correct.
OH
<
1
H₂SO4 +
HO
(O-S-OH
2
e
OH₂
8=S=O
3
UI
H₂O
0-S-OH
6
5
A. The dehydration reaction proceeds via an E1 mechanism.
B. Compound 6 is the most stable alkene formed by the dehydration.
C. The curved arrows, as shown in Compound 5, result in the formation of Compound 6.
D. Compound 6 is not the most stable alkene produced by the dehydration.
E. The dehydration reaction proceeds via an E2 mechanism.
K
Transcribed Image Text:Examine the reaction/mechanism provided for the acid-catalyzed dehydration of 2-methyl-2-butanol. Select all the following statements that are correct. OH < 1 H₂SO4 + HO (O-S-OH 2 e OH₂ 8=S=O 3 UI H₂O 0-S-OH 6 5 A. The dehydration reaction proceeds via an E1 mechanism. B. Compound 6 is the most stable alkene formed by the dehydration. C. The curved arrows, as shown in Compound 5, result in the formation of Compound 6. D. Compound 6 is not the most stable alkene produced by the dehydration. E. The dehydration reaction proceeds via an E2 mechanism. K
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