Q3. The main product of the following reaction is likely to be: CI CI CI hy A) a 4-membered cycloadduct B) a 6-membered cycloadduct C) a 7-membered cycloadduct D) a 5-membered cycloadduct
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- Rank the alkenes shown below based on stability, should be indicated as (most stable (left) to least stable right): i.e.: A > B > C > DIs the following alkene E,Z, or neither? a. E b. Z c. neither d. It is one or the other, but which is impossible to determine from the information given1. Which among these would be the most stable carbocation?a. Allylicb. Vinylicc. Primaryd. Secondary2. What is the primary reason for the stability of tertiary carbocations?a. Free rotationb. Resonancec. Hyperconjugation
- Carbocations often rearrange, as shown below. Draw in the hydrogens on the two carbons involved in the rearrangement, and show formal arrow-pushing to illustrate the transformation.Define Carbocation Stability?Classify the following carbocations as primary, secondary, tertiary, methyl, or vinyl carbocations as applicable: