[Review Topics] The two reactants shown below are combined to bring about a nucleophilic substitution reaction. a CH3 + CH3 b d KOCCH3 CH3 e. K+ f. "OC(CH3)3 g. 1 h. CH3OH Submit Answer i. HI j. "OH k. HOC(CH3)3 I. none [References] Which letter designates the electrophilic carbon at which substitution occurs? (If no reaction occurs enter the lette corresponding to "none.") Which letter corresponds to the leaving group? Which letter designates the nucleophile? Retry Entire Group 9 more group attempts remaining Previous

[Review Topics] The two reactants shown below are combined to bring about a nucleophilic substitution reaction. a CH3 + CH3 b d KOCCH3 CH3 e. K+ f. "OC(CH3)3 g. 1 h. CH3OH Submit Answer i. HI j. "OH k. HOC(CH3)3 I. none [References] Which letter designates the electrophilic carbon at which substitution occurs? (If no reaction occurs enter the lette corresponding to "none.") Which letter corresponds to the leaving group? Which letter designates the nucleophile? Retry Entire Group 9 more group attempts remaining Previous

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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QUESTION 2 The preparation of a Wittig salt from an alky halide and triphenylphosphine proceeds by a(n) O A. E2 O B. Sn2 OC. E1 O D. free radical O E. Sn1 mechanism. QUESTION 3 Which resonance structure is more reactive as a nucleophile? Ph Ph O A. 1 O B. 2 OC. both are equally reactive Click Save and Submit to save and submit. Click Save All Answers to save all answers. o search F10 F1 F2 F3 F4 F5 F6 23 2 3 4. 7 8 W Y UI
How to start this equation?
identify the type of nucleophilic substitution reaction it is (sn1 or sn2)
Choose the two alkyl bromides and the hydrogenation method that must be used to synthesize these alkenes from acetylene. Enter your answer as two letters in alphabetical order, followed by a number; i.e. ac2, not ca2. Do not use punctuation. Alkyl Halides a. CH3CH,Br. b. CH3(CH2)4Br c. CH3(CH2);Br d. CH3(CH2)6Br e. CH3(CH2);Br f. CH3(CH2);Br g. CH3(CH2)12B Hydrogenation Method 1. H2, Lindlar's catalyst 2. Na, NH3 (1) Alkene #1: H3C CH3 Alkene #2: CH3 H3C
9 [Review Topics] Draw the organic product(s) of the following reaction. 288 F4 V ÿ981 O % 5 You do not have to consider stereochemistry. • Draw one structure per sketcher. Add additional sketchers using the drop-down menu in the bottom right e T JUL 1 9 corner. . Separate multiple products using the + sign from the drop-down menu. B 6 OH II... + Fo Y ногон MacBook Air H tv Nall & 7 N 80 F7 Y C p-toluenesulfonic acid benzene, 80° * 00 Sn [F 8 K ChemDoodle DII FB I M [References] ♫AD ( 9 K DD FO O V O L 人口 O F10 P V ( F11 + { = [ Previous (211) F12 11 ? F Next> Save a 1 del
Choose the two alkyl bromides and the hydrogenation method that must be used to synthesize these alkenes from acetylene. Enter your answer as two letters in alphabetical order, followed by a number; i.e. ac2, not ca2. Do not use punctuation. a. CH3 CH₂ Br e. CH3 (CH₂)7 Br b. CH3 (CH₂)4 Br f. CH3 (CH2)8 Br c. CH3 (CH2)5Br g. CH3 (CH2) 12 Br d. CH3 (CH₂)6 Br Hydrogenation Method 1. H₂, Lindlar's catalyst 2. Na, NH3 (1) Alkene #1: Reagents available H₂C Alkene #2: H3C. CH3 CH3
Choose the two alkyl bromides and the hydrogenation method that must be used to synthesize these alkenes from acetylene. Enter your answer as two letters in alphabetical order, followed by a number; i.e. ac2, not ca2. Do not use punctuation. Alkyl Halides a. CH3CH₂Br b. CH3(CH₂)4Br c. CH3(CH2)sBr d. CH3(CH₂) Br e. CH3(CH₂)7Br f. CH₂(CH₂) Br g. CH3(CH₂)12Br Hydrogenation Method 1. H₂, Lindlar's catalyst 2. Na, NH3 (1) CH3 Alkene #1: H₂C Alkene #2: H₂C CH3
The two reactants shown below are combined to bring about a nucleophilic substitution reaction. Br CH;CH,CH,CHCH, NaOCH- e. Nao i. H20 HỌ. 'I g. "OCH3 h. НОCН3 j. HBr k. Br I. none Which letter designates the electrophilic carbon at which substitution occurs? (If no reaction occurs enter the letter corresponding to "none.") Which letter corresponds to the leaving group? Which letter designates the nucleophile? Submit Answer Retry Entire Group 9 more group attempts remaining
Choose the two alkyl bromides and the hydrogenation method that must be used to synthesize these alkenes from acetylene. Enter your answer as two letters in alphabetical order, followed by a number; i.e. ac2, not ca2. Do not use punctuation. Alkyl Halides а. СHзCH2Br b. CH3(CH2)4Br c. CH3(CH2)5Br d. CH3(CH2)§Br e. CH3(CH2);Br f. CH3(CH2)¿Br g. CH3(CH2)12Br Hydrogenation Method 1. H2, Lindlar's catalyst 2. Na, NH3 (1) Alkene #1: CH3 H3C bb1 Alkene #2: H3C, CH3 df1
te Bb Welcome, Kawtha... Maps News Home GE [Review Topics] [References] 1. Br H,SO, /H,O H20 Mg2+ Br HSO, 2. OH Na HCO, O Na CO2 H20 h = Sy1 Nucleophilic substitution i= SN2 Nucleophilic substitution- j= Electrophilic aromatic substitution a = Proton transfer e = Electrophilic addition b = Lewis acid/base f= El Elimination c = Radical chain substitution d = Radical chain addition g = E2 Elimination Identify the mechanism by which each of the reactions above proceeds from among the mechanisms listed. Use the letters a - j for your answers. 2. Submit Answer Retry Entire Group 9 more group attempts remaining Previous Next Email Instructor Save and Exi Cengage Learning | Cengage Technical Support
10. What is the major organic product obtained from the following reaction? b. 1 b. 2 k. 13 -CEN 1. NaOH. H₂O 2 H₂O* 3 NOH "NH₂ OH NH₂ 11. Which of the following substituents is ortho/para directing and deactivating in electrophilic aromatic substitution reactions? COCH, |b.NH, c. Br d. CH₂CH
14. Draw the line-bond structure of the product(s) formed in each reaction. LO-H + HO plan. + HN .. H+ heat - H₂O