2. X is a potential leaving group and could be displaced by the following reaction. Indicate...
4. X is a potential leaving group and could be displaced by the following reaction. Indicate if X is displaced when a. CH2CH3 b. Br C. OH and d. OCOCH
i need help with 2 please 1. Provide de ou treatment with aqueous base, on ase. . + oH + H₂O -OM R + oH - +he + oH 2. X is a potential leaving group and could be displaced by the following reaction Indicate if X is displaced when a H, b.CI or c. NH, (justify your choice). 3. Suggest reagents that could be used to prepare (2 methods) from an aldehyde or ketone.
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 explain why or why not A B C and D can be displaced! thanks! 4. X is a potential leaving group and could be displaced by the following reaction. + X Indicate if X is displaced when a. CH CH3 161.. b. Br c. OH and d. OCOCH3
3. Indicate the nucleophilic group and the electrophilic group in each of the following reactions, then draw curved arrows to show the electron flow: (a) H- N H -CH: (D) - (C) NH :CI: CI-APë: :CA: 1-ci: A-CI: 4. The following reaction has a small, positive AG and takes place slowly at room temperature: H3C-CI H-OH - H3C-OH - H-CI (a) The mechanism for the reaction is shown below. Which bond is being broken in the slowest step? Which bond...
1. What is the nucleophile in the following S2 reaction and what is the leaving group Br + NaCN 2. What are products of the following sequences of elementary steps? ci 1. Proton transfer involving NaOH 2. Nucleophile elimination 3. Nucleophilic addition of CH,MgBr 4. Sy2 involving CH Br (c) 1. Electrophilic addition of C 2. Electrophile elimination of HC (b) 1. E2 involving NaOCH, 2. Electrophilic addition involving H 3. Coordination involving H20 4. Proton transfer involving H2O OH...
a)indicate the reaction mechanism(s) favored by the particular type of leaving group, substrate, nucleophile/base, and solvent employed; b) predict the major pathway(s) that will occur under these conditions; c) provide the structure(s) of the major product(s) of the reaction ко Ме Me HT H Br Me-N Ме., 'H Me ко Ме Me HT H Br Me-N Ме., 'H Me
1. What is the nucleophile in the following S2 reaction and what is the leaving group? + NaCN 2. What are products of the following sequences of elementary steps? 1. Proton transfer involving NaOH 2. Nucleophile elimination 3. Nucleophilic addition of CH Mgr 4. Sy2 involving CH Br 1. Electrophilic addition of Ci 2. Electrophile elimination of H3C (b) (c) 1. E2 involving NaOCH, 2. Electrophilic addition involving H™ 3. Coordination involving H2O 4. Proton transfer involving H 0 осн,...
3. Indicate the nucleophilic group and the electrophilic group in each of the following reactions. then draw curved arrows to show the electron flow: H H-N: H-CI: Н (a) H-N H Н (b) HJ - :0: :O: (c) Cl: Cl-APCI: C : H-CI: A-CI: CF: 4. The following reaction has a small, positive AG and takes place slowly at room temperature:
For the following reaction, label the nucleophile, electrophile, and leaving group, Br + + Br Nucleophile Select] Electrophile (Select] Leaving Group [Select] For each of the following pairs, indicate with molecule is the better (stronger) nucleophile. [Select] [ Select] Z-I [Select) [Select]