Register
5. Write the two resonance hybrids for the carbocation that would be formed by protonation at C-1 of 2-methyl-1,3-pentadiene. Without doing a calculation, would you expect C-2 or C-4 (the two end carbons
36.6k views
3 votes
5. Write the two resonance hybrids for the carbocation that would be formed by protonation at C-1 of 2-methyl-1,3-pentadiene. Without doing a calculation, would you expect C-2 or C-4 (the two end carbons of the allylic cation) to have the most positive charge on it

User Mako
by
5.3k points

1 Answer

10 votes

Answer:

Follows are the solution to this question:

Step-by-step explanation:

Please find the complete solution in the attached file.

5. Write the two resonance hybrids for the carbocation that would be formed by protonation-example-1
User JustHooman
by
5.4k points
Ask a Question
Welcome to QAmmunity.org, where you can ask questions and receive answers from other members of our community.

5.6m questions

7.3m answers

Other Questions

How many pounds in a 3.00 l bottle of drinking water?
Compound A is an organic compound which contains Carbon, Hydrogen and Oxygen. When 0.240g of the vapour of A is slowly passed over a large quantity of heated Copper (II) oxide, CuO, the compound A is completely
Chlorine (Cl) forms a salt when it is combined with a metal. This element belongs in _____. group 18 group 17 period 18 period 17
In the following diagram for preparation of hydrogen gas as shown in the figure,what would happen if the following changes are made? (a) In place of zinc granules, same amount of zinc dust is taken in
When one substance changes into one or more new substances, it has exhibited a 1. chemical change. 2. chemical reaction. 3. physical change. 4. chemical property?
Link Copied!