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Question 3 Given your knowledge of the Wharton Reaction how would you convert the molecule on the left to the one on the right and what is the mechanism? op HO THE BIG BONU S QUESTION IS HOW WOUL...
a) What is the mechanism? b) If you were doing this reaction in lab, how would...
a) What is the mechanism?
b) If you were doing this reaction in lab, how would you use IR
to determine if you formed the product or a mixture of product and
starting material?
Question #1: Consider the reaction given, How would the reaction shift? Options are no change, right,...
Question #1: Consider the reaction given, How would the
reaction shift? Options are no change, right, or left.
Question #2: Determine if the above reaction is endothermic or
exothermic based on the following information. Is it endothermic or
exothermic?
Question #3: Explain your reasoning.
Consider 2 NBr3() = N2(8) + 3 Br2() How would the reaction shift if: [N2] is decreased: [Br2] is increased: The amount of N Br3 is doubled: The pressure is decreased by changing the volume: The...
Question 3 20 pts If you were monitoring the reaction of trans-stilbene being convert to stilbene...
Question 3 20 pts If you were monitoring the reaction of trans-stilbene being convert to stilbene dibromide via TLC, and under UV visualization you saw all three lanes, starting material / co-spot/ reaction, had visible spots, and when treated with KMnO4 and heated spots in all three lanes were yellow, what would you conclude. O The reaction had not gone to completion yet. O The reaction was complete. O You failed to spot the TLC plate with a concentrated enough...
You are given one starting material which is treated with 3 different condition. Determine the product(s)...
You are given one starting material which is treated with 3 different condition. Determine the product(s) that would be formed in each situation. Make sure to pay attention to stercochemistry!! NOTE: You must write down the problem and draw out the products on a separate sheet of paper. Take a picture make sure that it is clear) and upload it to this problem 1) BHz, THE 2) H302, NaOH HO HO 1) Hg(OAc), CH,OH 2) NaBH4, H20
O2F19-Quiz 9-Closed Book Acid and its derivatives 10/24/19-Name: Suggest how you would synthesis the following, Please...
O2F19-Quiz 9-Closed Book Acid and its derivatives 10/24/19-Name: Suggest how you would synthesis the following, Please use "big" arrow and go "backward". Start with final product and propose a route to make it Need to show all steps including arrows. Product on left side and starting material/intermediate on the right side. : Retrosynthesis is the process of "deconstructing" a target. molecule into readily available starting materials by ginary breaking of bonds (disconnections) and by the conversion of one functional group...
Q2-Predict the product(s) of the following reaction. What mechanism will this reaction follow? Would you expect...
Q2-Predict the product(s) of the following reaction. What mechanism will this reaction follow? Would you expect this reaction to go easily (fast)? Explain your answers related to the mechanism and the rate of the reaction. CH,OH Q3-Circle only basic nitrogen atoms in the following structures. Q4 - Give the IUPAC name for the following molecule. o OH NO2 Q5 - Draw the structures of the following compounds. 2,6-dibromo-4-chloroanisole m-nitroacetophenone
22. Show how you would make the target compounds on the right form the starting compounds on the left. Show reagent...
22. Show how you would make the target compounds on the right form the starting compounds on the left. Show reagents and conditions where appropriate, and the structures of important intermediate compounds. Do not show any (arrow pushing) mechanisms!!!! (8 points) NH2 3-Steps NH2 17. Show the products and give reaction mechanisms for the following, using curved arrows to indicate the flow of electrons between intermediates.
3. Given what you now know, what product(s) would you expect to isolate from this reaction?...
3. Given what you now know, what product(s) would you expect to isolate from this reaction? Y & NOT (NaO1-Bu) Specify how each of the following would affect the rate of the reaction. a. Increase the concentration of the base. b. Decreasing the concentration of alkyl halide.
3. Given what you now know, what product(s) would you expect to isolate from this reaction?...
3. Given what you now know, what product(s) would you expect to isolate from this reaction? Y +Na + Nao + - Br (NaOf-Bu) Specify how each of the following would affect the rate of the reaction. a. Increase the concentration of the base. b. Decreasing the concentration of alkyl halide. 3. Predict the product(s) for each of the E2 elimination reactions below. major product for each. heat Br NaOCH3 heat
3. Given what you now know, what product(s) would you expect to isolate from this reaction?...
3. Given what you now know, what product(s) would you expect to isolate from this reaction? • Ngô – Br (NaOt-Bu) Specify how each of the following would affect the rate of the reaction. a. Increase the concentration of the base. b. Decreasing the concentration of alkyl halide. 3. Predict the product(s) for each of the E2 elimination reactions below. Identify the major product for each. Y ahoo Br NaOCH heat
a) What is the mechanism?
b) If you were doing this reaction in lab, how would you use IR
to determine if you formed the product or a mixture of product and
starting material?
Question #1: Consider the reaction given, How would the
reaction shift? Options are no change, right, or left.
Question #2: Determine if the above reaction is endothermic or
exothermic based on the following information. Is it endothermic or
exothermic?
Question #3: Explain your reasoning.
Consider 2 NBr3() = N2(8) + 3 Br2() How would the reaction shift if: [N2] is decreased: [Br2] is increased: The amount of N Br3 is doubled: The pressure is decreased by changing the volume: The...
Question 3 20 pts If you were monitoring the reaction of trans-stilbene being convert to stilbene dibromide via TLC, and under UV visualization you saw all three lanes, starting material / co-spot/ reaction, had visible spots, and when treated with KMnO4 and heated spots in all three lanes were yellow, what would you conclude. O The reaction had not gone to completion yet. O The reaction was complete. O You failed to spot the TLC plate with a concentrated enough...
You are given one starting material which is treated with 3 different condition. Determine the product(s) that would be formed in each situation. Make sure to pay attention to stercochemistry!! NOTE: You must write down the problem and draw out the products on a separate sheet of paper. Take a picture make sure that it is clear) and upload it to this problem 1) BHz, THE 2) H302, NaOH HO HO 1) Hg(OAc), CH,OH 2) NaBH4, H20
O2F19-Quiz 9-Closed Book Acid and its derivatives 10/24/19-Name: Suggest how you would synthesis the following, Please use "big" arrow and go "backward". Start with final product and propose a route to make it Need to show all steps including arrows. Product on left side and starting material/intermediate on the right side. : Retrosynthesis is the process of "deconstructing" a target. molecule into readily available starting materials by ginary breaking of bonds (disconnections) and by the conversion of one functional group...
Q2-Predict the product(s) of the following reaction. What mechanism will this reaction follow? Would you expect this reaction to go easily (fast)? Explain your answers related to the mechanism and the rate of the reaction. CH,OH Q3-Circle only basic nitrogen atoms in the following structures. Q4 - Give the IUPAC name for the following molecule. o OH NO2 Q5 - Draw the structures of the following compounds. 2,6-dibromo-4-chloroanisole m-nitroacetophenone
22. Show how you would make the target compounds on the right form the starting compounds on the left. Show reagents and conditions where appropriate, and the structures of important intermediate compounds. Do not show any (arrow pushing) mechanisms!!!! (8 points) NH2 3-Steps NH2 17. Show the products and give reaction mechanisms for the following, using curved arrows to indicate the flow of electrons between intermediates.
3. Given what you now know, what product(s) would you expect to isolate from this reaction? Y & NOT (NaO1-Bu) Specify how each of the following would affect the rate of the reaction. a. Increase the concentration of the base. b. Decreasing the concentration of alkyl halide.
3. Given what you now know, what product(s) would you expect to isolate from this reaction? Y +Na + Nao + - Br (NaOf-Bu) Specify how each of the following would affect the rate of the reaction. a. Increase the concentration of the base. b. Decreasing the concentration of alkyl halide. 3. Predict the product(s) for each of the E2 elimination reactions below. major product for each. heat Br NaOCH3 heat
3. Given what you now know, what product(s) would you expect to isolate from this reaction? • Ngô – Br (NaOt-Bu) Specify how each of the following would affect the rate of the reaction. a. Increase the concentration of the base. b. Decreasing the concentration of alkyl halide. 3. Predict the product(s) for each of the E2 elimination reactions below. Identify the major product for each. Y ahoo Br NaOCH heat
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