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Compound W shows stereoisomerism.
- Why are such isomers formed in approximately equimolar quantities no matter the synthetic pathway used for the preparation of the compound?
![The diagram below shows two synthetic pathways by which the compound W might be prepared.
C3H;OH
C2H5OH
[0] P
[o] S
Q C3HGO2
T CH4O
Cl2
U.V.V
R C3H5O2CI
V C3H5ON
V
W CH;CH(OH)CO;H
Standing over Concentrated H2SO4](/v2/_next/image?url=https%3A%2F%2Fcontent.bartleby.com%2Fqna-images%2Fquestion%2Fc4ada34d-d86b-4fff-b27e-93764233fcc0%2F8afba86e-aeb9-4e68-b4b8-887bc8017357%2Fyap23sc_processed.jpeg&w=3840&q=75)
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- What is the expected major product for the following reaction? O IV I OCH 3 |||||... + enantiomer || 1. Hg(OAc)2, CH3OH 2. NaBH4 НО. OH ... H3CO. + enantiomer ||| IV H3CO V6. Complete reaction scheme below indicating reagents, catalysts and conditions, and side product trigil bezinslog si6101fon 290b 1l (b Senines levirba 6 gaubong nasamots gniwollot ads to doinW 01 sniowl (6 CH3 40 CH3 Scansgowi (d Ege nodie) ( nsgyxo (b NO₂ 19m02 2i gniwollet sits to mainW II HO2. Draw a reaction mechanism to explain the following reaction. O OH i. OH (aq) LOH
- 28. What is the major organic product of the following reaction? HO CI 1. (CH₂)₂Culi 2. H₂O A) I B) II C) III D) IV i c III ноха IV4. What are the products obtained from the following elimination reaction? Indicate the major product. CH;CH2CCH3 H2O CI 5. a) Determine the major product that is formed when the alkyl halide reacts with a hydroxide ion in an elimination reaction. CH;CH,CH,CH,CCH3 Br b) For the major elimination product obtained in 5a), which stereoisomer (cis or trans) is obtained in greater yield? Draw the two isomers and provide the names of the compounds.OMe O OMe mechanism requires PdCl₂ (cat) A CUCI, O₂ H₂O
- ) Starting from benzent synthesigo the fo lloning compounds. çooH NO2 NO2 NO2 NO2 BrPlace the product of each reaction in the next to conditions. Снз мамна гед THE DC H3CX CH3 вк вг Natt Et₂0,0°CPredict the product(s) for the following reaction. O ll + enantiomer I OI ||| OH O IV OH CN OH + enantiomer || 1. NaCN 2. H₂O CN "ОН + enantiomer ||| IV CN CNFor the reaction below, which one of the following possible products is most likely to form? (CH3)3CONA THE Br https://ibb.co/4TPJ2LH e https://ibb.co/2s1mWP9 2 https://ibb.co/fHsfhft a https://ibb.co/y0Cn8jY OcICHals https://ibb.co/CtzHTbx 2 https://ibb.co/ZghTKD6 eintermediates/products for this reaction Supply the missing . Please Show all 24.49. arrow pushimed Méchansmsi Mg(s). 1.8 Br2 Na,Cr,0z H2SO, SOCI, A B FeBr3 2. H300 AICI, Thanto ga! OCH3 Conc. H3PO4 → G OCH3 H. NABH4. ELOH ACH;O In the substitution reaction: (S)-2-bromononane CH;OH The product(s) of the reaction is(are)? OCH, OCH3 OCH3 A mixture of the major product c with the minor product d A equimolar mixture of b and c.SEE MORE QUESTIONS