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.
What reagent could accomplish this reaction?
Propose a successful synthesis of 1-decene from 1-bromodecane. Be sure to include specific reagents and solvents.
Select the best reaction conditions for the reaction below:
a) NaOCH3, DMSO
b) cat. H+, NaOCH3, CH3OH
c) cat. H+, NaOCH3, DMSO
d) NaOCH3, CH3OH
Complete the following reactions by indicating the missing product(s), or starting material.Show the stereochemistry when necessary.