The order of reactivity with grignard reagent is,
Acedic H>CHO>CO>COCl>COOR
In the first reaction, ester gives a tertiary alcohol.
In the second reaction, only one equivalent RMgX is there. Hence, alcohol H reacts with alkyl group to give alkane I.e, benzene.
In the third reaction first acid H reacts with RMgX and produces CH4. The second equivalent reacts with aldehyde to give secondary alcohol.
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 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...
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. Predict the major product in each of the following transformations. No mechanisms are required for this question. [3 Marks] 1. CH,сн,МgBr (еxcess) 2. HС{aq) 1. PhMgBr (1 equiv.) 2. HCI(aq) ОН HO 1. CH2MgBr (2 equiv.) 2. HCl(aq) Н Show how...
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 whether they are nucleophiles, electrophile, oxidizing, reducing agent or none. 1) Predict whether each of the reagents would be primarily one of the following: a nucleophile, an electrophile, an oxidizing reagent, a reducing agent or none. (0.5 points each.) OsO4 H, KMnO4 CH3MgBr CH,-Cl C3Hg KOH NaCN For the following reactions, predict the major product. Assume that reagents dded are in excess when required. You do not need to show mechanisms (2 points ach). MgBr 1) 1) Predict whether...
Predict the product of the following reaction AlCl3 Predict the product of the following reaction excess PhMgBr,then dilute acid Predict the product of the following reaction Ac2O,Et3N Predict the product of the following reaction Predict the product of the following reaction Predict the product of the following reaction 1 equiv. Ac2O Predict the product of the following reaction excess Ac2O Predict the product of the following reaction AlCl3Predict the product of the following reaction excess Ac2O Predict the product of...
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
Question : Predict the major product(s) for the following reaction EINH, Question 8 Predict the major product(s) for each of the following reactions: 1) RCO,H 2) [H,SOJ, CH,CH,OH Question : Identify the structure of the starting alkene in the following case: CH3 1) O CH4 2) DMS HyC Question 10 Predict the reagents and conditions that you would use to accomplish each of the following transformations: HC сн, -CH₂ HC
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.
Name Topic: Reaction Mechanisms: Predict your ability: For each of the following reactions, predict the major and minor product, underlining the major product. After, draw a complete arrow-pushing mechanism to obtain each product. СНЗ Good Average Needs Improvement 1. H30+, H20 CH S. CH Br2, H2O