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2. Consider the reaction of 3-methyl-2-pentene with HBr: HBr Show the mechanism and give the product...
Answer them accordingly thank you! Question 1 a) Give the mechanism for the reaction below: 3-ethyl-3-methyl-1-pentene + HBF3-bromo-3-ethyl-2-methylpentane b) The questions are based on the reaction scheme as shown below: H202 BH3 NaOH, H20 i) Determine the structure of intermediate A and product B. ii) The formation of product B follow one rule in electrophilic addition. What is the name of the rule and explain that rule. i) Give one reagent that can be used to reduce the alkyne above...
Part 1What is the major product of the following reaction? a. 2-ethyl-1-pentene b.(E)-4-methyl-3-hexene c.(E)-3-methyl-2-hexene d. (Z)-3-methyl-2-hexene Part 2 What alkyl chloride gives the following as the only product upon treatment with a strong base? a. b. c. d. Part 3 Give the major product for the following E1 reaction. a. b. c. d. e. CH3 CH3CO Br CH3
each a. 3-methyl-2-pentene b. cyclohexene с. propene 1.64 Give the name for the product from the hydrogenation of ead of the following: (11.7) a. 1-hexene b. 2-methyl-2-pentene cyclopropene 65 Draw the condensed structural or line-angle formula for the product of each of the following: (11.7) 19 Ni + H2 a. + H.O H b. mula for the 66 Deaw h.
3. Give the structures of the two products for addition reaction of HCl to 3-methyl-1-pentene (1 point). Point out which one is the major product, and explain why! (Hint: don t forget carbocation rearrangement)
3. Give the structures of the two products for addition reaction of HCI to 3-methyl-1-pentene (1 point), Point out which one is the major product, and explain why! (Hint: dont forget carbocation rearrangement) 4. The transformation of the alkyl chloride shown below into the alcohol can be accomplished in two steps. Show the synthetic scheme to finish the conversion. (1 point) OH
Bonus 3. Give the structures of the two products for addition reaction of HCl to 3-methyl-1-pentene (1 point). Point out which one is the major product, and explain why! (Hint: dont forget carbocation rearrangement) 4. The transformation of the alkyl chloride shown below into the alcohol can be accomplished in two steps. Show the synthetic scheme to finish the conversion. (1 point) Он Br
Propose a mechanism for this reaction. + Br2 + H2O 1-Pentene он Br + HBr 1-Bromo-2-pentanol
Show the reaction of 2-methyl-2-pentene and (CF3CO2)2Hg/CH3CH2OH followed by NaBH4. Show the products of the reaction of your ether in #4 and acid.
3. Give the major product for the following reactions. Proper stereochemistry (shape, geometry) is required / chirality may be ignored. Watch out for carbocation rearrangement, and proper geometry like cis/trans. (Be sure to check your work by working out reaction mechanisms - practice, practice, practice!) a. 2-methyl-1-pentene + HBr b. 2-methyl-1-pentene + HBr/peroxide c. 3-methyl-1-pentene + H30+
3. Give the major product for the following reactions. Proper stereochemistry (shape, geometry) is required / chirality may be ignored. Watch out for carbocation rearrangement, and proper geometry like cis/trans. (Be sure to check your work by working out reaction mechanisms - practice, practice, practice!) a. 2-methyl-1-pentene + HBr b. 2-methyl-1-pentene + HBr/peroxide c. 3-methyl-1-pentene + H30+ d. 3-methyl-1-pentene + 1. Hg(OAc)2/ROH 2. NaBH e. 2-methyl-1-pentene + 1. BH3, THF, 2. H202/OH-/H20 f. 3-methyl-1-cyclohexene + Brz, H20 g. 3-methyl-1-cyclohexene +...