For my lab, we have homework questions about the grignard reaction
1) If I start with 2-pentyl bromide, what would be the structure and name of the "impurity that could have formed during the preparation of the Grignard reagent.
I believe that the chief impurity would be 4,5-dimethyloctane.
2) Provide methods for synthesizing the following compounds using only a Grignard reaction, plus any necessary workup. In each case the Grignard reagent, propylmagnesium bromide, must be used in the synthesis. Express these syntheses in the form of balanced equations, using structural formulae, showing all reagents any specific conditions required
a) butanoic acid
b)1-pentanol
c)propane
d)4-ethyl-4-heptanol
e)4-ethyl-4-heptanol (different from d)
butanoic acid can be made from the grignard reagent as the starting material and then treating it with carbon dioxide and then having an acidic workup
1-pentanol can be made from an epoxide then use the reagents 1)PrMgBr, anh diethyl ether
2)H2O
for propane, I can just treat the grignard reagent with water to make propane
For 4-ethyl-4-heptanol, I can only think of one method and that is to use 3-hexanone as the starting material, use the grignard reagent to attack the 3-hexanone and then have an acidic workup.
Is this all correct so far? What other method could I use to make 4-ethyl-4-heptanol?