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please make it easy to read ( no cursive) thank you :) 4. If (R)-2-bromo-3-methylbutane were...
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...
please make it easy to read (no curisive) thank you ! :) 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 9 4 6 7 8 1 3 5 0 2
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
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 O . -45 -70 -95 - 120 0 2 4 6 8 10
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
Please make it easy to read (no cursive) THANK YOU SO MUCH :) 1. Draw the Sn1, SN2, Es, and Ez reaction mechanisms of (just do all four reactions for each): A. (R)-2-bromo-1-phenylpropane reacting with sodium hydroxide B.(2S,3R)-3-bromo-2-methoxy-3-methylpentane with NaF 2. If the two above reactions (from question 1) were carried out in DMSO at room temperature, which reaction mechanism would be favored and why? 3. Draw the most stable chair conformation of 1-t-butylcyclohexane
Please make it easy to read (no cursive) THANK YOU SO MUCH :) 7. Is it possible to tell if the following reaction took place via an E, or an E2 reaction? Explain why? H CH, H H Н. Base ΠΗ X + CH Br H 8. What is the majority product from the following Ez reaction, why? Br 9. Describe all of the reaction conditions necessary to complete the following reaction. Draw the mechanism. Оснэ
Please make it easy to read (no cursive) THANK YOU SO MUCH :) 10. Which solvent (acetone or t-butyl alcohol) would be better to carry out the following reaction? Why? Draw the complete mechanism of this reaction using generic base B. O 0 11. Name the following compounds F Ph NH ... H NH2 Bn
Please make it easy to read (no cursive). Thank you so much! :) 5. Draw the Newman Projection for butane in the gauche position. 6. Out of the following compounds, rank in terms of increasing heat of combustion?
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