Last Hydroboration Oxidation is an Anti-markovnikov additon of -OH group to alkyne, followed by tautomerization to form the desired aldehyde product. :-)
4. Show how the compounds below can be made in two ways in one reaction from the appropriate starting materials a)...
3. Show how the compounds below can be made in two different ways in a single step (one reaction from the appropriate starting materials. a Grignard reagent an epoxide a different epoxide analoohol an alkyl halide an alkene a bromoalcohol a different bromoalcohol
3. Show how the compounds below can be made in two different ways in a single step (one reaction) from the appropriate starting materials. the Ste a) a Grignard reagent a Grignard reagent OH an epoxide a different epoxide b) an alcohol a diene c) OH an alkyl halide an alkene d) a bromoalcohol 2 a different bromoalcohol
show how the compounds below can be made in two different ways in a single step (one reaction) from the appropriate starting materials an alcohol a diene
please help with all answers!! 3. Show how the compounds below can be made in two different ways in a single step (one reaction) from the appropriate starting materials. a Grignard reagent OH a Grignard reagent an epoxide a different epoxide an alcohol a diene an alkyl halide an alkene a bromoalcohol a different bromoalcohol
3. Devise S2 reactions that would lead to the following products. Show stereochemistry where relevant. CH DMF + NaBr nucleophile alkyl halide N сн,он nucleophile alkyl halide THF LICI nucleophile alkyl halide 4. Show how the compounds below can be made in two ways in one reaction from the appropriate starting materials. a) a cuprate a different cuprade b) an alkene an alkyne
wing 6 Show how the following compounds could be prepared from the given starting materials. You can use any necessary organic or inorganic reagents. NHCH -NH; CH OH OH ible or an inyersible reaction? Explain.
Question 3 Show how you can synthesize the following compounds using the indicated starting materials and any other necessary substances or reagents. (20 pts) A. CH COOH (starting from ortho-nitrotoluene) B. HN (starting from nitrobenzene)
Q 2. Show how each of the following compounds can be prepared from the given starting materials using retrosynthetic analysis approach. a) Available starting materials (source of carbon) H CH3NO2 Available starting materials (source of carbon)
Q 1. Show how each of the following compounds can be prepared from the given starting materials using retrosynthetic analysis approach. Available starting materials (source of carbon) a) .CO2Et CO2Et Ph Br CO2 or NaCN EtOH Ph CO2Et
Q 3. Show how each of the following compounds can be prepared from the given starting materials using retrosynthetic analysis approach. a) Available starting materials (source of carbon) CO2Et OH OPMB TM BrCH2COOEt OH OH p-methoxybenzaldehyde