Give the IUPAC name for the following compound.  

What is the expected product for the following reaction?   

Which of the following statements is consistent with the mechanism for nucleophilic addition of aldehydes/ketones under basic conditions?

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 three spaces between each step) All chemicals and reagents  structures should be correct and with the proper sequence. No partial credit.

Consider the partial rate factors for electrophilic aromatic substitution at the indicated position of anisole and nitrobenzene. Which of the following correlates to these partial rate factors (you may compare each of them to benzene)?

What is the structure for 5-hydroxy-2-phenyl-3-hexanone?

Predict the effect the substituent attached to the benzene ring below would have on electrophilic aromatic substitution reactions.

Which of the following is the most reactive toward addition of a Grignard reagent?

Which of the following is the reactive intermediate formed in the electrophilic bromination of toluene with Br2, FeBr3?

Identify the correct IUPAC name of the compound below.