propose a synthesis for the molecule starting with organic molecules containing no more than 8 carbons and provide the mechanistic steps using electron pushing arrows.

Give the product (b) of the synthesis shown.

Consider the reaction scheme below. (a) Name the reagent and conditions necessary for steps I to VI above. (b) Write balanced equations for step I to VI above. elow. 4. Consider the reaction scheme below. CH, CH CH₂CI III --------ပုံ CH₂OH CHÍNH, VI CH₂NHCOCH,CH, (a) Name the reagent and conditions necessary for steps I to VI above. (b) Write balanced equations for step I to VI above.

Hi, it's just one question but 3 subparts, and you are only allowed to answer up to 3 sub-parts please show the work clearly for all. Thank You

Suggest a synthesis of the following alkene using a Wittig reaction strategy. Clearly draw the starting materials and the full reaction mechanism. Comment on stereochemistry. Me Ph

Give me answer complete and with explanation how to right please.

Synthesis. Developments in medicine follows advances in synthetic chemistry. Anyone that disagrees would perhaps be well served to imagine the state of surgery if organic chemists had not developed local anesthetics. The following structure is the free base of hexylcaine (1), a local anesthetic developed by Merck. Propose a synthesis of 1 starting (1) from benzene and acyclic components containing five carbons or less. Justify any chemo-, regio- or stereo selective steps in your synthesis. (