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1. 2. O Na + Na CN toluene = tho.. + reflux DMF CH3 на мен он CN NaCl

1. 2. O Na + Na CN toluene = tho.. + reflux DMF CH3 на мен он CN NaCl

Chemistry
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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1. 2. O Na a = Electrophilic addition b = E2 Elimination c = SN1 Nucleophilic substitution 1. 2. Na CN Submit Answer -tho. toluene reflux DMF CH3 HZ, OH H₂CH CN + d = SN2 Nucleophilic substitution e= Electrophilic aromatic substitution f = Carbonyl nucleophilic addn Identify the mechanism by which each of the reactions above proceeds from among the mechanisms listed. Use the letters a - i for your answers. Retry Entire Group 9 more group attempts remaining NaCl g= Nucleophilic subs at carbonyl(acyl Xfer) h = Conjugate (nucleophilic) addn
Transcribed Image Text:1. 2. O Na a = Electrophilic addition b = E2 Elimination c = SN1 Nucleophilic substitution 1. 2. Na CN Submit Answer -tho. toluene reflux DMF CH3 HZ, OH H₂CH CN + d = SN2 Nucleophilic substitution e= Electrophilic aromatic substitution f = Carbonyl nucleophilic addn Identify the mechanism by which each of the reactions above proceeds from among the mechanisms listed. Use the letters a - i for your answers. Retry Entire Group 9 more group attempts remaining NaCl g= Nucleophilic subs at carbonyl(acyl Xfer) h = Conjugate (nucleophilic) addn
1. 2. N(CH3)31 1. 2. H₂O a = Electrophilic addition b = E2 Elimination C = SN1 Nucleophilic substitution KOH Submit Answer dilute H₂SO4 -OH + KI + d = SN2 Nucleophilic substitution e Electrophilic aromatic substitution f = Carbonyl nucleophilic addn Identify the mechanism by which each of the reactions above proceeds from among the mechanisms listed. Use the letters a - i for your answers. Retry Entire Group 9 more group attempts remaining N(CH3)3 + H₂O g = Nucleophilic subs at carbonyl(acyl Xfer) h = Conjugate (nucleophilic) addn
Transcribed Image Text:1. 2. N(CH3)31 1. 2. H₂O a = Electrophilic addition b = E2 Elimination C = SN1 Nucleophilic substitution KOH Submit Answer dilute H₂SO4 -OH + KI + d = SN2 Nucleophilic substitution e Electrophilic aromatic substitution f = Carbonyl nucleophilic addn Identify the mechanism by which each of the reactions above proceeds from among the mechanisms listed. Use the letters a - i for your answers. Retry Entire Group 9 more group attempts remaining N(CH3)3 + H₂O g = Nucleophilic subs at carbonyl(acyl Xfer) h = Conjugate (nucleophilic) addn
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