![organic chemistry - Can the nitrogen of an amide displace a primary chloride in a SN2 reaction in the presence of a strong base? - Chemistry Stack Exchange organic chemistry - Can the nitrogen of an amide displace a primary chloride in a SN2 reaction in the presence of a strong base? - Chemistry Stack Exchange](https://i.stack.imgur.com/SsiUJ.png)
organic chemistry - Can the nitrogen of an amide displace a primary chloride in a SN2 reaction in the presence of a strong base? - Chemistry Stack Exchange
![SOLVED: 1) NaOMe, MeOH OMe 2) H3O' , heat OMe (2 equiv:) 2) LAH MezCuLi Brz " (excess) NaOH (excess) SOLVED: 1) NaOMe, MeOH OMe 2) H3O' , heat OMe (2 equiv:) 2) LAH MezCuLi Brz " (excess) NaOH (excess)](https://cdn.numerade.com/ask_images/18f66ea52c574a438d427563644332ab.jpg)
SOLVED: 1) NaOMe, MeOH OMe 2) H3O' , heat OMe (2 equiv:) 2) LAH MezCuLi Brz " (excess) NaOH (excess)
![Scheme 2. Nucleophilic addition of NaOMe onto 1: acetal formation under... | Download Scientific Diagram Scheme 2. Nucleophilic addition of NaOMe onto 1: acetal formation under... | Download Scientific Diagram](https://www.researchgate.net/profile/Gabriel-Cabrera-4/publication/316335512/figure/fig1/AS:553189097574400@1508901966947/Scheme-2-Nucleophilic-addition-of-NaOMe-onto-1-acetal-formation-under-basic-conditions_Q320.jpg)
Scheme 2. Nucleophilic addition of NaOMe onto 1: acetal formation under... | Download Scientific Diagram
![When we use a base in a reaction, why is it always preferred to use the conjugate as the solvent? For example, if NaOMe is my base, the solvent will be HOMe . When we use a base in a reaction, why is it always preferred to use the conjugate as the solvent? For example, if NaOMe is my base, the solvent will be HOMe .](https://homework.study.com/cimages/multimages/16/a032185549421858048409.png)
When we use a base in a reaction, why is it always preferred to use the conjugate as the solvent? For example, if NaOMe is my base, the solvent will be HOMe .
![Scheme 3 Reagents: (a) NaOMe, MeOH; (b) MeI, NaH, THF; (c) TsCl, Et 3... | Download Scientific Diagram Scheme 3 Reagents: (a) NaOMe, MeOH; (b) MeI, NaH, THF; (c) TsCl, Et 3... | Download Scientific Diagram](https://www.researchgate.net/publication/244520295/figure/fig6/AS:371407172194310@1465561778434/Scheme-3-Reagents-a-NaOMe-MeOH-b-MeI-NaH-THF-c-TsCl-Et-3-N-DMAP-CH-2-Cl-2.png)
Scheme 3 Reagents: (a) NaOMe, MeOH; (b) MeI, NaH, THF; (c) TsCl, Et 3... | Download Scientific Diagram
![Which of the following would be the best base for performing the following elimination? A. NaOH B. NaOMe C. KOtBu D. H2O | Homework.Study.com Which of the following would be the best base for performing the following elimination? A. NaOH B. NaOMe C. KOtBu D. H2O | Homework.Study.com](https://homework.study.com/cimages/multimages/16/capture_13-27073458656355853889.jpg)
Which of the following would be the best base for performing the following elimination? A. NaOH B. NaOMe C. KOtBu D. H2O | Homework.Study.com
![Scheme 2. Nucleophilic addition of NaOMe onto 1: acetal formation under... | Download Scientific Diagram Scheme 2. Nucleophilic addition of NaOMe onto 1: acetal formation under... | Download Scientific Diagram](https://www.researchgate.net/publication/316335512/figure/fig1/AS:553189097574400@1508901966947/Scheme-2-Nucleophilic-addition-of-NaOMe-onto-1-acetal-formation-under-basic-conditions.png)
Scheme 2. Nucleophilic addition of NaOMe onto 1: acetal formation under... | Download Scientific Diagram
![SOLVED: (20 points, 2 each) Provide the major organic product of each reaction. Stereochemistry is unimportant NaOMe 2.EtBr OH Meo OMe 3. H3O COz base Hzot DCC OH aniline 1. LDA OH SOLVED: (20 points, 2 each) Provide the major organic product of each reaction. Stereochemistry is unimportant NaOMe 2.EtBr OH Meo OMe 3. H3O COz base Hzot DCC OH aniline 1. LDA OH](https://cdn.numerade.com/ask_images/487fb451dd6140379c1fd11cf889338a.jpg)