![SOLVED: What major product results from the following E2 reaction? NaOMe MeOH Br With the small base of NaOMe, will the base remove a proton from the beta-CH2 or beta-CH when deriving SOLVED: What major product results from the following E2 reaction? NaOMe MeOH Br With the small base of NaOMe, will the base remove a proton from the beta-CH2 or beta-CH when deriving](https://cdn.numerade.com/ask_images/c48046f817ee405687f72d30f4a03fc7.jpg)
SOLVED: What major product results from the following E2 reaction? NaOMe MeOH Br With the small base of NaOMe, will the base remove a proton from the beta-CH2 or beta-CH when deriving
![SOLVED: What is the major elimination product obtained from the following reaction? NaOMe Br MeOH 1. Identify the order of the alkyl halide (1,2,3) 2. What is the Nucleophile or Base? 3. SOLVED: What is the major elimination product obtained from the following reaction? NaOMe Br MeOH 1. Identify the order of the alkyl halide (1,2,3) 2. What is the Nucleophile or Base? 3.](https://cdn.numerade.com/ask_images/d234fed2035f4e088699770c9a8692df.jpg)
SOLVED: What is the major elimination product obtained from the following reaction? NaOMe Br MeOH 1. Identify the order of the alkyl halide (1,2,3) 2. What is the Nucleophile or Base? 3.
![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 .
![if we had used NaOMe instead of T-BuOK,wouldn't we have ended with the same product? since we have only on Beta postion? : r/chemhelp if we had used NaOMe instead of T-BuOK,wouldn't we have ended with the same product? since we have only on Beta postion? : r/chemhelp](https://preview.redd.it/hc90y6ldpoa31.png?width=640&crop=smart&auto=webp&s=bc8ef01fdbb3127531f5c5de0337292d49b830d8)
if we had used NaOMe instead of T-BuOK,wouldn't we have ended with the same product? since we have only on Beta postion? : r/chemhelp
![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
![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
![Here Meoh is used as a solvent and NaOMe is used as a nucleophile...then why is the product and elimination product rather than a substitution product?Thank u in advance community😁 : r/OrganicChemistry Here Meoh is used as a solvent and NaOMe is used as a nucleophile...then why is the product and elimination product rather than a substitution product?Thank u in advance community😁 : r/OrganicChemistry](https://preview.redd.it/tehs81sw78s71.jpg?width=640&crop=smart&auto=webp&s=11423bef3db685ae81c29ee67e83740cdd9df95c)