1) Predict the major product in each of the following transformations. Show the mechanism.
2) Show how you could synthesize the products below using a Grignard reagent and appropriate electrophile by drawing the overall balanced equation. Include the mechanism.
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1) Predict the major product in each of the following transformations. Show the mechanism. 2) Show...
Predict the major product in each of the following transformations. No mechanisms are required for this...
Predict the major product in each of the following
transformations. No mechanisms are required for this question.
Predict the major product in each of the following transformations. No mechanisms are required for this question. [3 Marks] 1. CH,CHMgBr (excess) hoy 2. HCl(aq) i 1. PhMgør (1 equiv.) 1. PhMgBr (1 equiv.) 2. HCl(aq) охон 1. CH3MgBr (2 equiv.) 2. HCl(aq) Show how you could synthesize the products below using a Grignard reagent and appropriate electrophile by drawing the overall balanced...
Predict the major product in each of the following transformations. No mechanisms are required for this...
Predict the major product in each of the following transformations. No mechanisms are required for this question. [3 Marks] 1. CH3CH2MgBr (excess) 2. HCl(aq) 1. PhMgBr (1 equiv.) 2. HCl(aq) ОН о но 1. CH3MgBr (2 equiv.) 2. HCl(aq) н Show how you could synthesize the products below using a Grignard reagent and appropriate electrophile by drawing the overall balanced equation. No mechanisms are required for this question. You do not need to show formation of the Grignard reagent. [2...
Predict the major product in each of the following transformations. No mechanisms are required for this...
Predict the major product in each of the following transformations. No mechanisms are required for this question. [3 Marks] 1. CH CH MgBr (excess) 2. HCl(aq) 1. PhMgBr (1 equiv.) 2. HCl(aq) OSOH 1. CH_MgBr (2 equiv.) 2. HCl(aq)
Show how you could synthesize the products below using a Grignard reagent and appropriate electrophile by...
Show how you could synthesize the products below using a Grignard reagent and appropriate electrophile by drawing the overall balanced equation. No mechanisms are required for this question. You do not need to show formation of the Grignard reagent. [2 marks] HO H3COH Ph Phi
Show how you could synthesize the products below using a Grignard reagent and appropriate electrophile by...
Show how you could synthesize the products below using a
Grignard reagent and appropriate electrophile by drawing the
overall balanced equation.
НО не он PhPh.
Predict the major product of each of the following reactions. Postlab Questions: Predict the major product...
Predict the major product of each of the following
reactions.
Postlab Questions: Predict the major product of each of the following reactions. Alkyl lithium reagents function in the same manner as Grignard reagents 1. 1) 2 PhMgBr 2) H30+ 1) 2 BuLi Cl 2) H30 1) 2 MeMgl 2) H3O 1) 2 EtMgCl 2) H3O* OH 1) 2 PhMgBr 2) H 0
1. predict the major products. 2. draw detailed arrow mechanism. 1. Predict the major product of...
1. predict the major products.
2. draw detailed arrow mechanism.
1. Predict the major product of the reaction. Clearly indicate stercochemistry, if necessary На Lindlarca Me hexanes 2. Provide reagents to achieve the shown multi-step transformations (6 pts)
also show the mechanism and curved arrows for each mechanism 2. Predict the products for the...
also show the mechanism and curved arrows for each
mechanism
2. Predict the products for the reaction between le products for the reaction between Br, as well as Br/H, and the Alkenes listed below. rredict whether each reaction is syn- or anti-, Label the substrate, nucleophile and electrophile in each reaction. Substrate Structure Overall Reaction with Brz (with products) syn- or Overall Reaction with Bry/H20 (with products) anti- 3,3-dimethyl-1-1 butene 1-hexene styrene (phenylethene)
I. (40 points) Predict the major product(s) for each of the following transformations. Be sure to...
I. (40 points) Predict the major product(s) for each of the following transformations. Be sure to indicate stereochemistry and draw enantiomers when appropriate. Clearly show stereochemistry with two lines in the plane and a wedge or dash at the chirality center. No reaction mechanisms are necessary.
HELP PLEASE ANSWER ALL III. Predict the major product(s) or fill in the reagent(s) for the...
HELP PLEASE ANSWER ALL
III. Predict the major product(s) or fill in the reagent(s) for the following reactices. If there is to reaction write NR. (6 points each, 16 points total) Show the correct stresshemistry when needed!! 16 H.CO (excess) CHO HO 17 10 (equiv.) 2) Mes (2 equis.) 18 OH o" 19 1) mCPBA 2) EXON, EICH 20 1) LIAIR (excess) io 2) H 0,1,0 21 1) SNI, 2) CH, Br 3) HBr (2 equiv.) 22.Draw DETAILED arrow.pushing mechanisms...
Predict the major product in each of the following
transformations. No mechanisms are required for this question.
Predict the major product in each of the following transformations. No mechanisms are required for this question. [3 Marks] 1. CH,CHMgBr (excess) hoy 2. HCl(aq) i 1. PhMgør (1 equiv.) 1. PhMgBr (1 equiv.) 2. HCl(aq) охон 1. CH3MgBr (2 equiv.) 2. HCl(aq) Show how you could synthesize the products below using a Grignard reagent and appropriate electrophile by drawing the overall balanced...
Predict the major product in each of the following transformations. No mechanisms are required for this question. [3 Marks] 1. CH3CH2MgBr (excess) 2. HCl(aq) 1. PhMgBr (1 equiv.) 2. HCl(aq) ОН о но 1. CH3MgBr (2 equiv.) 2. HCl(aq) н Show how you could synthesize the products below using a Grignard reagent and appropriate electrophile by drawing the overall balanced equation. No mechanisms are required for this question. You do not need to show formation of the Grignard reagent. [2...
Predict the major product in each of the following transformations. No mechanisms are required for this question. [3 Marks] 1. CH CH MgBr (excess) 2. HCl(aq) 1. PhMgBr (1 equiv.) 2. HCl(aq) OSOH 1. CH_MgBr (2 equiv.) 2. HCl(aq)
Show how you could synthesize the products below using a Grignard reagent and appropriate electrophile by drawing the overall balanced equation. No mechanisms are required for this question. You do not need to show formation of the Grignard reagent. [2 marks] HO H3COH Ph Phi
Show how you could synthesize the products below using a
Grignard reagent and appropriate electrophile by drawing the
overall balanced equation.
НО не он PhPh.
Predict the major product of each of the following
reactions.
Postlab Questions: Predict the major product of each of the following reactions. Alkyl lithium reagents function in the same manner as Grignard reagents 1. 1) 2 PhMgBr 2) H30+ 1) 2 BuLi Cl 2) H30 1) 2 MeMgl 2) H3O 1) 2 EtMgCl 2) H3O* OH 1) 2 PhMgBr 2) H 0
1. predict the major products.
2. draw detailed arrow mechanism.
1. Predict the major product of the reaction. Clearly indicate stercochemistry, if necessary На Lindlarca Me hexanes 2. Provide reagents to achieve the shown multi-step transformations (6 pts)
also show the mechanism and curved arrows for each
mechanism
2. Predict the products for the reaction between le products for the reaction between Br, as well as Br/H, and the Alkenes listed below. rredict whether each reaction is syn- or anti-, Label the substrate, nucleophile and electrophile in each reaction. Substrate Structure Overall Reaction with Brz (with products) syn- or Overall Reaction with Bry/H20 (with products) anti- 3,3-dimethyl-1-1 butene 1-hexene styrene (phenylethene)
I. (40 points) Predict the major product(s) for each of the following transformations. Be sure to indicate stereochemistry and draw enantiomers when appropriate. Clearly show stereochemistry with two lines in the plane and a wedge or dash at the chirality center. No reaction mechanisms are necessary.
HELP PLEASE ANSWER ALL
III. Predict the major product(s) or fill in the reagent(s) for the following reactices. If there is to reaction write NR. (6 points each, 16 points total) Show the correct stresshemistry when needed!! 16 H.CO (excess) CHO HO 17 10 (equiv.) 2) Mes (2 equis.) 18 OH o" 19 1) mCPBA 2) EXON, EICH 20 1) LIAIR (excess) io 2) H 0,1,0 21 1) SNI, 2) CH, Br 3) HBr (2 equiv.) 22.Draw DETAILED arrow.pushing mechanisms...
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