reactions

draw the structures of the indicated products

Alkene and Alkyne Mechanisms

In my organic class we are studying alkenes and alkynes. I am familiar with the addition and elimination procedures. However, I am unclear of how some of the mechanism go since my book only deals with the straight forward mechanisms such as halogenation, hydration, etc.

Organic Chemistry Questions

Please see attachment for questions A to E. Please explain in detail (11 Credits Bid).

Organic Chemistry

Please view attachment.

stereochemistry

What is the absolute stereochemistry of the asymmetric carbon in compound O? When compound O is treated with lithium diisopropyl amide, followed by allyl bromide, compound P is produced as a single stereoisomer. What is the absolute stereochemistry of the newly produced asymmetric carbon in P? Provide concise explanations for ...continues

conformers

Which conformer, K or L is predicted to be more stable? Explain your answer (Assign the absolute (R or S) configurations for each of the chiral carbons in carbohydrates M and N. Are either of these compounds optically active? Briefly explain your answer.

Practice exercise

I attempted some of this but I am clueless as to some of the other stuff. Can you help?

Missing materials

please see attached document

synthesis

Synthesize the following compound You may also use any organic compounds containing three or less carbon atoms, benzene, N-bromosuccinimide, triphenylphosphine, meta-chloroperbenzoic acid (MCPBA), methylvinyl ketone, lithium diisopropylamide (LDA), ethyl acetoacetate (acetoacetic ester) and diethyl malonate (malonic ester), as ...continues

synthesis

Synthesize the following compound from the indicated starting material. You may also use any organic compounds containing three or less carbon atoms, benzene, N-bromosuccinimide, triphenylphosphine, meta-chloroperbenzoic acid (MCPBA), methylvinyl ketone, lithium diisopropylamide (LDA), ethyl acetoacetate (acetoacetic ester) and ...continues