Draw the major product of this reaction. Include stereochemistry if applicable. Use a dash or wedge bond to indicate the stereochemistry of substituents on asymmetric centers, where applicable. Ignore byproducts. Q CI CHзONa heat Br
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- Draw the major prodct from this reaction. Use a dash and/or wedge bond to indicate the stereochemistry of substituents on asymmetric centers, where applicable. Ignore acid byproducts. mCPBA < On Q 000 Atom anc Draw or MacBDraw the final product of this series of reactions. |||** OH 1. SOCI₂ 2. NaCN • Use the wedge/hash bond tools to indicate stereochemistry where it exists. • If more than one product is possible, only draw the major product. • If the reaction produces a racemic mixture, draw both stereoisomers.Determine the mechanism of nucleophilic substitution of each reaction and draw the products, including stereochemistr CH₂CH3 CI Br + CN d. + CH3COOH a. acetone + -OCH3 e. DMF f. b. C. ||||| a ||||| Br H Br CH2CH2CH3 + CH3OH DMSO H CH3 CI Br + OCH₂CH3 + CH3CH₂OH
- Draw the major prodct from this reaction. Use a dash and/or wedge bond to indicate the stereochemistry of substituents on asymmetric centers, where applicable. Ignore acid byproduct. Incorrect, 1 attempt remaining 1. Br2, H₂O 2. NaOH 0Use the References to access important values if needed for this question. Draw the structure of the product that is expected when the following compound is treated with concentrated H2SO4. он H2S04 ? heat CH3 You do not have to consider stereochemistry. • In cases where there is more than one answer, just draw one. ited opy Bste [F CH4 ChemDoodle Retry Entire Group 3 more group attempts remaining Submit Answer Previous Next Email Instructor Save and Exit Cengage Learning | Cengage Technical SupportPlease show the mechanism for this reaction. Show lone pairs, charges, and proper arrow placement. What is the minor and major product and why? Also, draw a Newman Projection of EACH of the benzoin products. Include a scheme analyzing the relative stereochemistry of the diol products (which are enantiomers/diastereomers/meso compounds) and labelling the isomers using R/S notation. No explanation required for the R/S notation OH NABH4 ОН ient:
- ew fopics] Draw the major organic product of the reaction shown below. H2SO4 HO, • You do not have to consider stereochemistry. • You do not have to explicitly draw H atoms. • In cases where there is more than one answer, just draw one. C opy aste [F ChemDoodleIdentify the major product of the reaction of an alkene shown below. ||| 1. Hg(OAc)2, H2O 2. NaBH4, NaOH ....... ОН || IV ОН о, ОНAlkene bromination. The two butane isomers react with Br2. Draw the key reaction inter- mediates and the product(s); use arrow pushing to explain the stereochemical outcomes of the reactions Final Products Intermediate Br2 Intermediate Final Products Br2
- 3) Explain how and why the reaction below results in the observed regiochemistryand/or stereochemistry.Draw the products of the following reactions, indicating both regiochemistry and stereochemistry when appropriate. Use wedge and hash bonds ONLY when needed to show reaction stereochemistry. In cases where there is more than one answer, just draw one.des and Nucleophiles atomic center possesses an excess of positive charge, it is more likely to react with regions with ess of negative charge. The center of positive charge "loves" regions with high electron density and Aus called electrophiles. When an atomic center possesses an excess of negative charge, it is more Ay to react with centers with an excess of positive charge. The center of negative charge "loves" egions where the nuclear charge is less shielded and are thus called nucleophiles. Generally, labelling a center as nucleophilic or electrophilic requires a fair amount of excess charge on that center and poor stabilization of the charge. Note that while the charge distribution on a molecule is a strong driver of how it will react, there are other factors that also matter. 7) For each molecule below, label any nucleophilic or electrophilic centers. Briefly explain your reasoning. a) b) c) OH Li NH₂ d) e) f) NⓇH -N- on nucleophilic strength. 8) For each molecule below, predict…