Why isn't Br replaced by OH-?
Please explain in detail.
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Why isn't Br replaced by OH-?
Please explain in detail.
The compound either A or B...
Please explain how to draw the newman projection as well. 2. Explain why the following compound...
Please explain how to draw the newman projection as well.
2. Explain why the following compound reacts to give a mixture of alkene stereoisomers in which only the cis-dimethyl isomer contains deuterium. Hint: draw the alkyl halide in a Newman projection. You will be asked to do this on midterm 1. Br CH,CH,OH Das * Change CACHON le CH3 C'H + CH3CH,0. H;c Stvong base
please explain it with details Many thanks One of the compounds (A) - (C) forms an...
please explain it with details
Many thanks
One of the compounds (A) - (C) forms an epoxide with base, but the other two form carbonyl compounds. Explain with mechanisms and clear 3-dimensional representations. Br Br OH OH OH
Can someone please answer and explain what the name of this compound is ? Br OH...
Can someone please answer and explain what the name of this
compound is ?
Br OH compound C name: 3-bromo-6-chloro-1-phenol
My teacher is that A is not the major product. please explain why and what would...
My teacher is that A is not the major product. please explain
why and what would be the major
22) (9 points) For the following reaction: a. (5 points) Draw a complete and detailed mechanism for the process shown below to form compounds A and B. mention whether it is initiation, propagation or termination. b/ (2 points) Explain why this reaction gives a mixture of compounds A and B and does not give compound C c. (2 points) Which product...
Please explain in full detail. 5. (16) Propose mechanisms to explain these transformations: Br NaOCH CH, OH heat
Please explain in full detail.
5. (16) Propose mechanisms to explain these transformations: Br NaOCH CH, OH heat
2. (1.5 Credits) a. One carbon in Compound A is an alpha carbon and beta carbon....
2. (1.5 Credits) a. One carbon in Compound A is an alpha carbon and beta carbon. Circle this carbon. b. Box the leaving group(s) in Compound A. If the leaving group is poor, how can it be made better? Br c. Compound A reacts with H SO4. Draw two possible intermediates of this reaction. Which intermediate most likely forms? Give reasons. d. One of your intermediates from part c forms Compound B. Use curved arrows to show how Compound B...
OH EtOH, H* OH Br 1, NaOH 2. HCI compound compound b poud c SOCh compound...
OH EtOH, H* OH Br 1, NaOH 2. HCI compound compound b poud c SOCh compound 0 OMe HN LIAIH compound d compound f Cyclomethycaine The above reaction scheme presents one possible synthesis of eyclomethycaine. Work out the synthesis on a separate sheet of paper, and then draw the structure of compound f.
The compound CH3NH2 reacts with water to form CH3NH3+ and OH-. On this reaction CH3NH2 acs...
The compound CH3NH2 reacts with water to form CH3NH3+ and OH-. On this reaction CH3NH2 acs as a(n) ____. (a) acid (b) base (c) salt (d) catalyst (e) solvent
Please explain a b c and d as to why or why not X is displaced....
Please explain a b c and d as to why or why not X is
displaced. Thanks in advance.
4. X is a potential leaving group and could be displaced by the following reaction. + X Indicate if X is displaced when a. CH2CH3 b. Br c. OH and d. OCOCH
Please show work and explain in detail. Thanks 2. 1) Select the reagents needed for the...
Please show work and explain in detail.
Thanks
2.
1) Select the reagents needed for the following reaction: a. H2, Pd-C b. HCI c. H2, Lindlar catalyst d. H2O, H2SO4 2) Consider the mechanism for acid-catalyzed hydration of alkenes. Select the intermediate(s) for the following reaction: H20, H2SO4 nyo yo'n M OH 3) Consider the mechanism for the halogenation of alkenes. Select the intermediate(s) for the following reaction: Br2 JBr + ...Br Br Br Br 11Br VuBr
Please explain how to draw the newman projection as well.
2. Explain why the following compound reacts to give a mixture of alkene stereoisomers in which only the cis-dimethyl isomer contains deuterium. Hint: draw the alkyl halide in a Newman projection. You will be asked to do this on midterm 1. Br CH,CH,OH Das * Change CACHON le CH3 C'H + CH3CH,0. H;c Stvong base
please explain it with details
Many thanks
One of the compounds (A) - (C) forms an epoxide with base, but the other two form carbonyl compounds. Explain with mechanisms and clear 3-dimensional representations. Br Br OH OH OH
Can someone please answer and explain what the name of this
compound is ?
Br OH compound C name: 3-bromo-6-chloro-1-phenol
My teacher is that A is not the major product. please explain
why and what would be the major
22) (9 points) For the following reaction: a. (5 points) Draw a complete and detailed mechanism for the process shown below to form compounds A and B. mention whether it is initiation, propagation or termination. b/ (2 points) Explain why this reaction gives a mixture of compounds A and B and does not give compound C c. (2 points) Which product...
Please explain in full detail.
5. (16) Propose mechanisms to explain these transformations: Br NaOCH CH, OH heat
2. (1.5 Credits) a. One carbon in Compound A is an alpha carbon and beta carbon. Circle this carbon. b. Box the leaving group(s) in Compound A. If the leaving group is poor, how can it be made better? Br c. Compound A reacts with H SO4. Draw two possible intermediates of this reaction. Which intermediate most likely forms? Give reasons. d. One of your intermediates from part c forms Compound B. Use curved arrows to show how Compound B...
OH EtOH, H* OH Br 1, NaOH 2. HCI compound compound b poud c SOCh compound 0 OMe HN LIAIH compound d compound f Cyclomethycaine The above reaction scheme presents one possible synthesis of eyclomethycaine. Work out the synthesis on a separate sheet of paper, and then draw the structure of compound f.
Please explain a b c and d as to why or why not X is
displaced. Thanks in advance.
4. X is a potential leaving group and could be displaced by the following reaction. + X Indicate if X is displaced when a. CH2CH3 b. Br c. OH and d. OCOCH
Please show work and explain in detail.
Thanks
2.
1) Select the reagents needed for the following reaction: a. H2, Pd-C b. HCI c. H2, Lindlar catalyst d. H2O, H2SO4 2) Consider the mechanism for acid-catalyzed hydration of alkenes. Select the intermediate(s) for the following reaction: H20, H2SO4 nyo yo'n M OH 3) Consider the mechanism for the halogenation of alkenes. Select the intermediate(s) for the following reaction: Br2 JBr + ...Br Br Br Br 11Br VuBr
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