1. C
2. E
3. A
4. B
5. D
I hope that helps <3
Answer:
6. d
7.c
8.a
9.b
Explanation:
For 6, the answers are not particularly close to 100, and they are not clustered much. For 7, the answers are all clustered very close to 100. For 8, the answers are clustered closely, but not close to 100. For 9, the answers are close to 100, but not clustered very tightly. Hope this helps!
<span>1,3-cylohexadiene i synthesized starting from cyclohexane in following 4 steps.
1) Free Radical Substitution Rxn: Halogenation of cyclohexane in the presence of UV yield chlorocyclohexane.
2) Elimination Rxn: Dehydrohalogenation of chlorocyclohexane yields cyclohexene.
3) Halogenation of Cyclohexene (
Electrophillic Addition Rxn) gives 1,2-dihalocyclohexane.
4) Elemination Rxn: When dibromocyclohexane is treated with KOH and heated it gives 1,3-cyclohexadiene as shown below,</span>