3. Show how the compounds below can be made in two different ways in a single step (one reaction from the appropria...
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
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
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
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 cuprate an alkyne an alkene
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
Show how the reaction of an allylic halide with a Grignard reagent might be used to synthesize the following hydrocarbons (draw two starting compounds; one allylic bromide and one Grignard reagent.) Make sure your Grignard is a bromide in problem. 1. 5-methylhex-1-ene 2. 2,5,5-trimethylhept-2-ene 3. 1-cyclopentylpent-2-ene
Tertiary alcohols with two identical alkyl groups attached to the alcohol carbon can be made either from an ester and two moles of a Grignard reagent, or from a ketone and one mole of a Grignard reagent. Use retrosynthetic analysis to suggest one path of each type to synthesize 3-methyl-3-pentanol. (Click and drag the appropriate image to the correct position in the following reactions.) Tertiary alcohols with two identical alkyl groups attached to the alcohol carbon can be made either...
Tertiary alcohols with two identical alkyl groups attached to the alcohol carbon can be made either from an ester and two moles of a Grignard reagent, or from a ketone and one mole of a Grignard reagent. Use retrosynthetic analysis to suggest one path of each type to synthesize 2-phenyl-2-propanol. (Click and drag the appropriate image to the correct position in the following reactions.) Tertiary alcohols with two identical alkyl groups attached to the alcohol carbon can be made either...
43. Tertiary alcohols with two identical alkyl groups attached to the alcohol carbon can be made either from an ester and two moles of a Grignard reagent, or from a ketone and one mole of a Grignard reagent. Use retrosynthetic analysis to suggest one path of each type to synthesize 1,1-diphenylethanol. (Click and drag the appropriate image to the correct position in the following reactions.) Tertiary alcohols with two identical alkyl groups attached to the alcohol carbon can be made...
Tertiary alcohols with two identical alkyl groups attached to the alcohol carbon can be made either from an ester and two moles of a Grignard reagent, or from a ketone and one mole of a Grignard reagent. Use retrosynthetic analysis to suggest one path of each type to synthesize 2-methyl-2-butanol. (Click and drag the appropriate image to the correct position in the following reactions.) Tertiary alcohols with two identical alkyl groups attached to the alcohol carbon can be made either...