4. If (R)-2-bromo-3-methylbutane were to react with water, describe reaction conditions of how the achiral compound 2-methylbutan-2-ol would form. Draw the mechanism
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4. If (R)-2-bromo-3-methylbutane were to react with water, describe reaction conditions of how the achiral compound...
please make it easy to read ( no cursive) thank you :) 4. If (R)-2-bromo-3-methylbutane were to react with water, describe reaction conditions of how the achiral compound 2-methylbutan-2-ol would form. Draw the mechanism. 6.What type of reaction happened if 3-chlorohexane reacted with water to form hexan-3-ol given the following chart and why? Draw the mechanism. Angle of light rotation as reaction proceeds 130 105 80 55 30 5 -20 -45 -70 -95 -120 . 0 1 2 3 4...
Please make it easy to read (no cursive) THANK YOU SO MUCH :) 4. If (R)-2-bromo-3-methylbutane were to react with water, describe reaction conditions of how the achiral compound 2-methylbutan-2-ol would form. Draw the mechanism. 5.Put the following three compounds in order of increasing basicity. OH OH OH 6.What type of reaction happened if 3-chlorohexane reacted with water to form hexan-3-ol given the following chart and why? Draw the mechanism. Angle of light rotation as reaction proceeds 130 105 80...
3) Complete the reactions to show the multi-step syntheses of each product from (R)-2 bromo-3-methylbutane. Reaction conditions go in boxes above arrows (1 reaction/box) Complete the template molecules provided to show each step of the synthesis. [20] Hint- This question involves addition, elimination, substitution and alcohol chemistry Br (R)-2-bromo-3-methylbutane 3-methylbutan-1-ol (R)-2-bromo-3-methylbutane (R)-3-bromo-2 methylbutan-2-ol (R)-2-bromo-3-methylbutane (1-chloro-2-methylbutane (R)-2-bromo-3-methylbutane CN ()-1-cyano-3-methylbutan-1-ol
Gradescope #2 This question is worth 10 points. The reaction between (R)-2-bromo-3-methylbutane and water in the presence of heat forms Br. H30* and two organic products. Draw a stepwise mechanism for this reaction, clearly showing how each product is formed. Use curved arrows to show electron movement, and include all reactive intermediates, resonance structures, etc. Br H20
Gradescope #2 This question is worth 10 points. The reaction between (R)-2-bromo-3-methylbutane and water in the presence of heat forms Br", H3O+ and two organic products. Draw a stepwise mechanism for this reaction, clearly showing how each product is formed. Use curved arrows to show electron movement, and include all reactive intermediates, resonance structures, etc. Br H2O Δ
(R)-2-iodo-3-methylbutane is treated with sodium bromide in acetone. Select all products that are formed.2-methylbut-2-ene(R)-3-methyl-2-butanol(S)-2-bromo-3-methylbutane3-methylbut-1-ene2-methylbutan-1-ol2-methylbutan-2-ol
Which would react fastest with 2-bromo-3-methylbutane in an E2 reaction? CH3Li CH2CH2NH2 CH3PH2 CH3CH2ONa CHCH NHNa A B co
Name the following compound. CÁCH Br. Н H CH CH.CH 1-bromo-1-methylbutane 1-bromo-2-methylbutane 3-bromo-2,4-dimethylhexane 4-bromo-2,2,3-trimethylhexane
5. Explain how the following changes will influence the rate of the reaction of 2-bromo-2- methylbutane with methanol: a. The alkyl halide is changed to 2-chloro-2-methylbutane b. The alkyl halide is changed to 2-chloro-3-methylbutane 6. What product(s) do you predict for the following reactions? Be specific with regard to stereochemistry. Also, indicate which stereoisomer will be more predominant. a. R-2-bromopentane + CH30 b. R-3-bromo-3-metylheptane + CH3OH C. 1-bromo-2-butene + CH30 d. 1-bromo-2-butene + CH3OH e. E2 reaction of 2-bromobutane f....
R)-2-iodo-3-methylbutane is treated with sodium hydroxide. Select all products that are formed.2-methylbutan-1-ol3-methylbut-1-ene(S)-3-methyl-2-butanol(R)-3-methyl-2-butanol2-methylbut-2-ene2-methylbutan-2-ol