The animals, climate, weather.
The answer is rings, I know this because i took a test about it and I got it right
Answer:
The answer to your question is below
Explanation:
Process
1.- Look for the longest chain
2.- Number the carbons of the main chain starting from the corner where the double bond is closer.
3.- Circle the branches
4.- Start naming the number where the branch is and the name of the branch.
5.- Name the main branch with the ending -ene.
5-methyl, 1-hexene or 5-methyl, hex-1-ene
See gthe structure below.
Answer:
See explanation
Explanation:
The mechanism of this reaction including intermediates are shown in the image attached to this answer.
The reaction of HBr with 3-bromocyclohexene yields trans-1,2-dibromocyclohexane as the sole product because; the proton first attacks the 3-bromocyclohexene and a brominium ion is formed. This brominium ion is a cyclic intermediate as shown in the image attached.
Attack of a bromine ion afterwards must lead to the formation of trans-1,2-dibromocyclohexane as shown.