subject
Chemistry, 12.02.2020 04:48 zlyzoh

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?

ansver
Answers: 2

Another question on Chemistry

question
Chemistry, 21.06.2019 19:00
If a || b and e || f, what is the value of y ?
Answers: 3
question
Chemistry, 22.06.2019 02:30
What is the mass of sodium in 3 moles of sodium chloride
Answers: 1
question
Chemistry, 22.06.2019 13:30
An animal cell loses the ability to convert energy stored in food to energy that the cell can use. which of the cell's organelles has stopped working? a.the mitochondria b.the nucleus c.the vacuoles d.the endoplasmic reticulum
Answers: 1
question
Chemistry, 22.06.2019 16:50
Which element is least likely to undergo a chemical reaction
Answers: 3
You know the right answer?
Write the two resonance hybrids for the carbocation that would be formed by protonation at C-1 of 2-...
Questions
question
Mathematics, 20.05.2021 20:50
question
Mathematics, 20.05.2021 20:50
question
Mathematics, 20.05.2021 20:50
question
Chemistry, 20.05.2021 20:50
Questions on the website: 13722362