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- Draw the curved arrow notation and predict the products when one equivalent of methoxide in DMSO a: rcom ten:perature is sdced to S-brome-1. 1odepentane. Part 1 ht See Periodic Table O See Hint DMSO Draw the curved arrow notation. Part 2 Select the major byproduct. Chooso one: O A, I- O B. HI O C. CH:OH O D Er. O E. Herew fopics] Draw the major organic product of the reaction shown below. H2SO4 HO, • You do not have to consider stereochemistry. • You do not have to explicitly draw H atoms. • In cases where there is more than one answer, just draw one. C opy aste [F ChemDoodleGve the major product of the following reaction. CH,CH,ONa H. HO. HO. L There is no reaction under these conditions or the cor«.Lproduct.is not fisted here,
- For the reaction below, draw he reachon mechanisms) (aurows) and predict al she major products. If no reachon will H2C acur brey explain whag: Br CH20HDraw the major organic product of the reaction shown below. Он H2SO4 You do not have to consider stereochemistry. • You do not have to explicitly draw H atoms. • In cases where there is more than one answer, just draw one. opy aste ChemDoodleDraw the major organic product of the reaction shown below. HO Hoa + HCI • You do not have to consider stereochemistry. • You do not have to explicitly draw H atoms. /n [F ? ChemDoodleⓇ
- The nitration reaction of the two compounds shown below is carried out. Draw in each case the majority product obtained OMe NO₂biackboard.gwu.edu/webapPps/assessment/feview/review.jsprattempld Select the major product of the reaction below. 1) TIPSCI, Et3N 2) Na 3) 03, then CH3SCH3 4) CH3CH2LI, then H30* 5) Bu4N* F', H2O CI Selected Answer: Он HO Answers: он он он OH OH OH он Select the major product of the reaction below. The answer is there, but please explain step by step.Draw the major organic product of the reaction shown below. O Ca OH **** + HBr • You do not have to consider stereochemistry. • You do not have to explicitly draw H atoms. - ] Jn [1 ChemDoodleⓇ 5b
- 2. Which of the following would give a meta product when submitted to EAS reaction conditions? OA OB OC OD OE OF A B C H CF3 E F CI HOWhat is the predicted product of the reaction shown? ОТ O II ||| O IV OV OH OH 1. 2. 3. Na2Cr2O7/H2SO4/H2O Оз DMS н || ОН он ОН Ш ее юля О НО IV V ОНc. Snl reactions dominate under polar protic solvents. Increasing the polarity of the solvent will increase the rate of the reaction because the polar solvent will stabilize the dispersed charges on the transition state more than it will stabilize the neutral reactant. Label areas of ô* and & on the molecules of the transition state of the SN1 reaction below: Me Me Ме Me Me H20 Br -Br OH + НО \'H Et Et RDS Et H Et Et transition state not isolable carbocation intermediate not isolable