1.2.CH3H₂C+B-BrCH3a Proton transferb = Lewis acid/basec = Radical chain substitution1.2.ICIC₂H5N-C₂H5C₂H5d = Radical chain additionElectrophilic additione =f = E1 EliminationC₂H5+1H-N-C₂H5 BrC₂H5g = E2 Eliminationh=SN1 Nucleophilic substitutioni = SN2 Nucleophilic substitutionIdentify the mechanism by which each of the reactions above proceeds from among themechanisms listed. Use the letters a - i for your answers.

reaction-1: The ICl is added to alkene. Reaction-2: alkene is produced from tertiary alkyl bromide…

1. 2. CH3 H3C- -Br CH3 1. + a = Proton transfer b = Lewis acid/base c = Radical chain substitution 2. ICI C₂H5 N-C₂H5 C₂H5 d = Radical chain addition e = Electrophilic addition f = E1 Elimination C₂H5 H-N-C₂Hs Br C₂H5 g = E2 Elimination h = Identify the mechanism by which each of the reactions above proceeds from among the mechanisms listed. Use the letters a - i for your answers. SN1 Nucleophilic substitution i = SN2 Nucleophilic substitution

1. 2. CH3 H3C- -Br CH3 1. + a = Proton transfer b = Lewis acid/base c = Radical chain substitution 2. ICI C₂H5 N-C₂H5 C₂H5 d = Radical chain addition e = Electrophilic addition f = E1 Elimination C₂H5 H-N-C₂Hs Br C₂H5 g = E2 Elimination h = Identify the mechanism by which each of the reactions above proceeds from among the mechanisms listed. Use the letters a - i for your answers. SN1 Nucleophilic substitution i = 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...

See similar textbooks

Similar questions

1. Reaction of excess methyllithium with ethyl acetate (CH3CO2C2H5) produces, after acid work-up, ___. 2. Reaction of excess ethyl magnesium bromide with ethyl benzoate (C6H5CO2C2H5) produces, after acid work-up, ___. 3. Reaction of excess ethyl magnesium iodide with ethyl acetate (CH3CO2C2H5) produces, after acid work-up, ___.
H Ph 1. HO NaOH Ph Br DMSO / H20 2. N-Br ..OH N-H a = Proton transfer d = Radical chain addition E2 Elimination b = Lewis acid/base e = Electrophilic addition h = SN1 Nucleophilic substitution Radical chain substitution f=E1 Elimination i= SN2 Nucleophilic substitution C = Identify the mechanism by which each of the reactions above proceeds from among the mechanisms listed. Use the letters a - i for your answers. 1. 2.
to 1. conc. HBr H20 Br OH O Na 2. Na NH2 NH3 d = El Elimination f = SN1 Nucleophilic substitution a = Proton transfer b = Lewis acid/base e = E2 Elimination g = SN2 Nucleophilic substitution c = Electrophilic addition 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. 1. 2. Submit Answer Retry Entire Group 8 more group attempts remaining
1. CH3 Ph oto KOH O OH Ethanol Ph Ph-H -CH₂ + KCI H₂O 2. OCOH a = Proton transfer d Radical chain addition g= E2 Elimination b= Lewis acid/base e Electrophilic addition h = SN1 Nucleophilic substitution c = Radical chain substitution f = E1 Elimination 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. 1. 2. HCI
EXPLAIN THE MECHANISM OF EACH REACTION 3. Hydrogen Addition- Selectivity CH₂ H₂C- Catalyst CH₂ HH 4. Mechanism of Catalytic Hydrogenation H H Alkane product ⒸThomson-Brooks Cole -H Pd H H Hydrogen adsorbed on catalyst surface Regenerated catalyst H₂C CH₂ H H C C LIZ Complex of alkene to catalyst Η Η΄ CH₂ H H H Insertion of hydrogen into carbon-carbon double bond
1. aq. NaOH reflux NaCI H20 OH 2. HI a = Proton transfer d = Radical chain addition g = E2 Elimination b = Lewis acid/base e = Electrophilic addition h = SN1 Nucleophilic substitution C = Radical chain substitution f = E1 Elimination 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. 1. 2. Submit Answer Retry Entire Group 9 more group attempts remaining
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 -
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
3 9 $ 4 R H₂C B % 5 1. Aqueous ethanol HBr CH₁ 2. OH a Proton transfer d E1 Elimination. f = SN1 Nucleophilic substitution b Lewis acid/base. e E2 Elimination g= SN2 Nucleophilic substitution c = Electrophilic addition 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. 1. 2. Submit Answer Retry Entire Group 9 more group attempts remaining Previous Next> Save and Exit Cengage Learning Cengage Technical Support O 8:15 AM 6/20/2022 PrtScn PgDn F5 F6 T B CH₂ Nà Nha ^ 6 Y H N & 7 [Review Topics] H₂C U 8 M CH₂ NH₂ K [References] H₂C 73°F Sunny Home ( 9 O L End 0 G F10 P PgUp 4x F12 □
Choose the reaction that will not proceed as written. OH H. 1) xs LIAIH4, ether a) H,C 2) H+, H20 NH2 b) H,C H3C HO, H3C CI pyridine OH H+ 1) xs CH3MgBr,ether + NH4+ + CH3CH2OH c) H3C H20 d) H;C NH2 OH OCH2CH3 2) H+, H20 H3C CH3 CH heat O b O a O d
1. MgBr 1. Dry ether OH 2. Hао 2. Br AIB 3 AIBra d = Electrophilic addition g = SN1 Nucleophilic a = Proton transfer substitution h = SN2 Nucleophilic b = Lewis acid/base e = El Elimination substitution c = Radical chain f= E2 Elimination 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. 1. 2. Submit Answer Retry Entire Group 8 more group attempts remaining
Criteria for satisfactory score Reactants, products, and reagents that complete a reaction scheme must specific compounds, not generic categories. Reagents and structures must be valid Lewis structures. Tasks Complete the synthetic sequences by drawing products/substrates/reagents in empty spaces in reactions below. 1. t-BUOK, heat 2. Br2 (1 equiv) methanol (solvent) Br 1. O3 2. Me2S 1. Hg(OAc)2, H2O 2. NABH4