the correct option is B
NaOH is a source of Hydroxide ion which is a strong Nucleophile which replaces Iodide ion by SN2 mechanism ,
The Bromine present on the ring does not get substituted by Hyroxide ion ,as Aromatic Nucleophillic Substitution does not occur at ordinary conditions.
Question 9 3 pts Predict the major organic product of the following reactions. Assume one equivalent...
Question 7 3 pts Predict the major organic product of the following reactions. Assume one equivalent of reagent unless otherwise stated, it's a solvent, oxidizing, or reducing agent. If no reaction will occur, choose E. Be mindful of stereochemistry 3. H2O, HCI
predict the major products of the following reactions Question 5 3 pts Predict the major organic product of the following reactions. Assume one equivalent of reagent unless otherwise stated, it's a solvent, oxidizing, or reducing agent. If no reaction will occur, choose E. Be mindful of stereochemistry ОН Next < Previous
no explanation needed, I just need the right answer choices. Thank you!! Predict the major organic product of the following reactions. Assume one equivalent of reagent unless otherwise stated, it's a solvent, oxidizing, or reducing agent. If no reaction will occur, choose E. Be mindful of stereochemistry. Me Me 1. Mgº, THE o Br Me H Me 1 Me 3. H20, HCI Me Y Me Me Me Me Me Me Me HO он Me Me Me Me Predict the major...
2. Predict the major organic product(s) of the reactions below. Assume 1 equivalent of reagent unless otherwise stated, it's a solvent, or an oxidizing/reducing agent. Do consider stereochemistry and regioselectivity. 2. Predict the major organic product(s) of the reactions below. Assume 1 equivalent of reagent unless otherwise stated, it's a solvent, or an oxidizing/reducing agent. Do consider stereochemistry and regioselectivity. (3 points each; 15 points total) A. Me 1. HNO3 2. O3 3. DMS 1. mCPBA, DCM (1 equiv) 2....
4. (6 pts) Predict the major product for the following reactions. Remember to indicate stereochemistry, when appropriate. Unless otherwise noted you may assume that each reagent is available in excess. If no reaction is expected, write NR. 1 H2O OTS NaSH ü Nash DMSO Br QB CH,OH CH3OH
3. Reactions: (21 pts) Draw the structure of the expected organic product(s) formed in the following reactions including correct stereochemistry, if the product is racemic indicate this by either drawing both enantiomers or drawing one and writing racemic. Assume all reagents listed are present in excess unless otherwise noted. If no reaction occurs, state ‘No Reaction'. HI H) 1) CHELI 2) H30 CrOg, H2SO4 H20 (xs) 1) mCPBA J) (CH3),COK (CH3)3COH CH,CI2 K) H2SO4 180°C OH L NaH, DMSO Br...
3. Reactions: (21 pts) Draw the structure of the expected organic product(s) formed in the following reactions including correct stereochemistry, if the product is racemic indicate this by either drawing both enantiomers or drawing one and writing racemic. Assume all reagents listed are present in excess unless otherwise noted. If no reaction occurs, state ‘No Reaction'. HI H) 1) CHELI 2) H30 CrOg, H2SO4 H20 (xs) 1) mCPBA J) (CH3),COK (CH3)3COH CH,CI2 K) H2SO4 180°C OH L NaH, DMSO Br...
3. Reactions: (21 pts) Draw the structure of the expected organic product(s) formed in the following reactions including correct stereochemistry, if the product is racemic indicate this by either drawing both enantiomers or drawing one and writing racemic. Assume all reagents listed are present in excess unless otherwise noted. If no reaction occurs, state 'No Reaction'. HI H) 1) CH3Li CrO3, H2SO4 1) H 2) H30+ H20 (xs) CI mCPBA (CH3)3COK J) (CH3)3COH CHCI2 K) H2SO4, 1800C OH Nah, DMSO...
Question 12 1 pts Predict the major product of the reaction below with one equivalent of NaOH in DMF, (DMF is a polar protic solvent) NaOH (1) DMF come and not (al hi 10 id U Question 13 1 pts What would be the major product formed from the transformation below?
8. Predict the major product or products for the following reactions. Assume reagents are present in excess amounts unless otherwise indicated. Clearly depict any stereochemistry. "No Reaction" is a possible answer. (4 points) each heat two products HBr ether KMnO4 H30