Bonus question Provide a stepwise synthesis for the following.      he answer should be entered as in the following example: (this is an example!) 1. NaNH2   2. CH3CH2Br   3. H2, Lindlar’s Cat.    4. BH3, THF   5. H2O2, NaOH                          (Keep five spaces between each step) All chemicals and reagents  structures should be correct and with the proper sequence. No partial credit.

Provide the product for the following reaction sequence.

Which one of the following is not an intermediate in the acid-catalyzed reaction of benzaldehyde with two equivalents of methanol to give benzaldehyde dimethyl acetal?

The 13C NMR spectrum of a compound with formula C7H14O shows five signals. Which one of the following is a possible structure for this compound?

Provide the product of the following reaction.    

Of the choices given, where would an aromatic substitution occur on this molecule?

What would be the product of the following reaction?

Bonus question What is the IUPAC name of the following compound?  

The 1H NMR spectrum of a compound with formula C7H14O shows a singlet at 9.2 ppm. Which one of the following is a possible structure for this compound?

Identify the products of the hydrolysis of the following compound.