1. 2. a Proton transfer b = Lewis acid/base c = Electrophilic addition 1. 1. BBr3 heat 2. H₂O 2. of OH CH₂Br B(OH)3 d = E1 Elimination e E2 Elimination KBr + HOCEt3 The rections above involve synthesis or reactions of alcohols and ethers. Identify the mechanism by which they proceed from among the mechanisms listed. Use the letters a - g for your answers. f = SN1 Nucleophilic substitution g = SN2 Nucleophilic substitution

1. 2. a Proton transfer b = Lewis acid/base c = Electrophilic addition 1. 1. BBr3 heat 2. H₂O 2. of OH CH₂Br B(OH)3 d = E1 Elimination e E2 Elimination KBr + HOCEt3 The rections above involve synthesis or reactions of alcohols and ethers. Identify the mechanism by which they proceed from among the mechanisms listed. Use the letters a - g for your answers. f = SN1 Nucleophilic substitution g = SN2 Nucleophilic substitution

Chemistry

10th Edition

ISBN:9781305957404

Author:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste

Publisher:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste

Chapter1: Chemical Foundations

Section: Chapter Questions

Problem 1RQ: Define and explain the differences between the following terms. a. law and theory b. theory and...

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Subject- chemistry
Solve both parts otherwise I will downvote
Part A Provide the major organic product(s) of the reaction below. H₂C CH 3 H3C H 1. LiAlH4 2. H¹, H₂O
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1. 2. ㅅ a = Proton transfer b Lewis acid/base C = Radical chain substitution = 1. 00 2. Br₂ CH3OH conc. HBr OCH 3 Br + OH d = O Radical chain addition e = Electrophilic addition f = E1 Elimination HBr Br E2 Elimination SN1 Nucleophilic substitution i = SN2 Nucleophilic substitution Identify the mechanism by which each of the reactions above proceeds from among the mechanisms listed. Use the letters a - i for your answers. 9 h -
Please help….in simple terms Because I’m very confused.
1. 2. CH3 a 1. www 2. CH3 + Br a = Proton transfer b = Lewis acid/base c = Radical chain substitution HCI مار Na benzene, reflux CH₂ d CI d Radical chain addition e = Electrophilic addition f = E1 Elimination 4 HO-CH + NaBr Identify the mechanism by which each of the reactions above proceeds from among the mechanisms listed. Use the letters a - i for your answers. g = E2 Elimination h = SN1 Nucleophilic substitution i = SN2 Nucleophilic substitution
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1. 2. H₂C 1. MeO 2. -CH3 H₂O a = Proton transfer b = Lewis acid/base c = Radical chain substitution H3PO4 80° MeO CH3 H₂COM₂ CH3 d = Radical chain addition e = Electrophilic addition f = E1 Elimination H₂O Identify the mechanism by which each of the reactions above proceeds from among the mechanisms listed. Use the letters a - i for your answers. g = E2 Elimination h = SN1 Nucleophilic substitution i = SN2 Nucleophilic substitution
Answer b,d,e part only
Suppose you are given the starting molecule shown below. For each of the cases listed below, list the reaction conditions and reagents that would give that product, and give a brief explanation of why ONLY the specified product would be formed under the conditions you chose. Make product alcohol with OH group at carbon 1. Make product alcohol with OH group at carbon 2. Make product alcohol with OH group at carbon 3. а. b. 3 2 C.
1. 2. Ph 1. Ph OH a Proton transfer b = Lewis acid/base c = Electrophilic addition 2. + Na CN NMe₂ DMF H₂SO4 Ph Ph H3C H CH3 H CN OH NM²₂ Tamoxifen anti (brest) cancer drug Ph d E1 Elimination = e = E2 Elimination Ph NMe₂ The rections above involve synthesis or reactions of alcohols and ethers. Identify the mechanism by which they proceed from among the mechanisms listed. Use the letters a- g for your answers. f = SN1 Nucleophilic substitution gSN2 Nucleophilic substitution