1. Predict the product(s) of the following SN2 reactions and include stereochemistry where necessary. Br КОН...
1. (20 points) Provide the product(s) for the following reactions. Provide stereochemistry where necessary. Determine whether they are SN2, S1, F2, E1, or Elcb where necessary. NO NEED FOR MECHANISMS. NaOCH.CH diethyl ether кожи DMSO We were unable to transcribe this image
1. Predict the major substitution product(s) for the following reactions. Include stereochemistry if appropriate. You may assume an aqueous workup is performed after each reaction. 1. Nah, DMF ТОН 2. Mel BrMg-Ph KCN 16 { ad ton ot MeOH HD Na Br Me DMSO EtOH Br ~ Br DMSO * Me OH LNH2 M HO Me-S (1 equiv) Me DMF
7. Predict the product(s) of each of the following reactions include stereochemistry where important and indicate the mechanism (S, S,2, El, E2). 80°C a 2-chloro-2-methylbutane NaOH Н.о b. (R)-2-chloropentane Nac c-H DMSO с1 (снс. Cн, CH,ОН d. trans-1-chloro-3-methylcyclohexane+ NaOC(CH) e. 2-chloro-3-phenylbutane Н.о f. trans-1-bromo-3-methyleyclopentane Nal acetone NaOCH THон g 2-chloro-2-methylbutane EIOH h R-3-bromo-2-methylpentane . trans-1-bromo-2-isopropyleyclohexane CHCOK NaSH Н,о j. 1-bromopropaе NaOCH снон CH коссH). I-bromobutane m. cis-1-chloro-3-methyleyclobutane Nal DMSO сHсH,он n. (R)-2-iodo-2-phenylethane NaOH o. 1-iodobutane p. 2-bromo-3-methylbutane KOC(CH). но (S)-3-chlorocyclopentene...
Of the following equations predict the product of the reactions. Include stereochemistry in cases where more than one product is formed . Circle the major product of the reaction 0 CH2CH3 Br CH13 0, HI (2 equivalents Он (1) NaH CH3CH2 Choosing reagents and reaction conditions of your choice, propose a two-step transformation of the given substrate Br Br KOCICH3)s (2 equiv)
please answer all 1. Draw the structure of the principal organic product and predict the stereochemistry to be expected from the reaction of (IR, 2R)-1-bromo-2-methylcyclohexane with each of the following: a. NaOCH, in CH,OH at 60° d. NaNH, in NH, at 50° b. aqueous CH,OH at 140° e. aqueous CH,CH,OH at 25° c. Nal in DMSO at 40° 2. Draw the major product(s) (showing appropriate stereochemistry when necessary) for the following reactions. Indicate the mechanism(s) in operation (SNI, SN2, E1,...
1. (20 points) Provide the products for the following reactions. Provide stereochemistry where necessary. Determine whether they are SN2, S1, E2, E1, or Elcb where necessary. NO NEED FOR MECHANISMS. Br NaOCH.CH diethyl ether KOBU DMSO heat NaCN THF
For the following set of reactions predict the major product(s). Underneath each product, state if they are by; SN1, SN2, E1, E2. Include stereochemistry where necessary
suggest the major product(s) for the following reactions. specify the stereochemistry clearly and write "racemic" for a racemic product. Br КОН heat BH3, THF NaOH, H2O2 NaN3 DMSO Br HCI SOH HBr
Predict the product(s), both major and minor, of the following reactions. Indicate stereochemistry where appropriate. Br. H Nang g DMF OH H2PO4 OMS KOC(CH3)3 HOC(CH3)3
Please do A. 1. Predict the product for the following reactions. Show stereochemistry where appropriate. A. H2NNH2 KOH, DMSO B. H30