Video Solution: Compound A (C6H14) gives three different monochlorides on ph...

Sign up for free to keep watching this solution
Organic Chemistry / Substitution/Elimination Retrosynthesis / Problem #18185

Compound A (C6H14) gives three different monochlorides on photochemical chlorination. One of these monochlorides is inert to E2 elimination. The other two monochlorides yield the same alkene B (C6H12) on being heated with potassium tert -butoxide in tert -butyl alcohol. Identify compound A, the three monochlorides,and alkene B.