degree of unsaturation for norethindrone Using acetylene any alkyl halides as starting materials, show how you...
1) Show how you might synthesize m-bromobenzoic acid, using benzene and any suitable catalyst as your starting materials. 2) Show how you might synthesize 2-methylhexane, using acetylene and any suitable alkyl halides as your starting materials.
2. Starting with any alcohols, phenols or alkyl halides you wish, show how each of the following can be prepared by the Williamson synthesis (HINT: The second step goes by the Sn2 mechanism.) a. Dipropyl ether b. ethyl butyl ether
Devise a synthesis of these compounds starting with 3-carbon alkyl halides. Show any necessary reagents and reaction conditions. All carbons must ultimately come from the 3-carbon alkyl halides. Once you have made a new compound, you may reuse it without making it again. a) Propanone b) Butanoic acid c) 3-hexene
1) Draw another more 3-resonance forms of the following: show the movement of the arrows, and charge for each HN NH2 2) Show how you might synthesize cis-2-methyl-3-hexene, using acetylene and any suitable alkyl halides and catalyst as your starting materials
8. Using acetylene as one of the starting materials, show the synthesis of the following compound a
Name 4. Starting with cyclohexene and acetylene as the only source of carbons, show a synthesis of the compound below. 1. Show how you could make the given product from the given starting material. Show all steps. OH a CECH 2. Starting with acetylene and methyl bromide as your only source of carbons show a synthesis of cis-2-butene. 5. Prepare 2-methoxy-propanol from 1-bromo-propane. Show the steps and use any reagents you need. 3. Using acetylene and propyl bromide as your...
Please answer in detail
8. Using acetylene as one of the starting materials, show the synthesis of the following compound
13. Using acetylene as one of the starting materials and any other reagents required, outline a synthetic route (including all reagents, proper order of addition and the product for each step) to obtain the following compound (with the stereochemistry shown):
10-2 Using acetylene as the starting material, show how you would synthesize the following compounds а) b) but-2-yne с) d)
(V) ! show the preparation of the following compounds
(v) 2-heptanone starting from acetylene (vi) Cis-3-hexene starting from acetylene D E Focus LE English (US) MacBook Pro