Choose the major product(s) of the following reaction. 

In the following multi-step synthesis: Describe the reaction that happens in step 1.  Explain or name the product in the middle box.   Describe the reaction that happens in step 2.  Propose the IUPAC name of the final product.        

Answer the following questions with complete explanations of your reasoning for each.  Which of the following fatty acids is most likely to be solid at room temperature?  Which of the fatty acids above would turn orange last upon addition of bromine?  CH3(CH2)4(CH=CH)CH2(CH=CH)(CH2)7COOH CH3(CH2)18COOH CH3(CH2)7CH=CH(CH2)6COOH CH3(CH2)16COOH

BONUS (5 points): Synthesize the product on the left from propyne and any other carbon source and any inorganic reagents needed.  Use retrosynthetic analysis to aid your thinking, however only the synthesis in the forward direction will be graded.  Indicate all reagents used as well as solvents when relevant.  You do not need to illustrate any mechanisms. Name the product using IUPAC nomenclature.

Which descriptor best fits the site indicated by an arrow below?  

Label each indicated alkene as E or Z in the molecule below.

Choose the major product(s) of the following reaction. 

The intermediate for the mechanism for the halogenation reaction shown should be [intermediate] leading to [stereo] stereoselectivity for the product.

Answer the following questions with complete explanations of your reasoning for each.  Which of the following fatty acids is most likely to be solid at room temperature?  Which of the fatty acids above would turn orange last upon addition of bromine?  CH3(CH2)4(CH=CH)CH2(CH=CH)(CH2)7COOH CH3(CH2)18COOH CH3(CH2)7CH=CH(CH2)6COOH CH3(CH2)16COOH

Choose the major product(s) of the following reaction.