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- Draw the organic product of the following reaction. CH3 m-CICgH,CO;H • Use the wedge/hash bond tools to indicate stereochemistry where it exists. • If the reaction produces a racemic mixture, just draw one stereoisomer. • If more than one product is possible, only draw the major product. opy asteWhich carbocation is the most stabilized? Me Me CO₂Me MeO A B C D Select an answer and submit. For keyboard navigation, use the up/down arrow keys to select an answer. a A b B CC OMe Me Me OMe Me Me MeO. OMe E Me MeDraw the organic product of the following reaction. H₂C-CH₂-C CH ● 1 NaH2 2. CH₂CH₂Br • You do not have to consider stereochemistry. • You do not have to explicitly draw Hatoms.
- Draw the major elimination and substitution products formed in this reaction. Use a dash or wedge bond to indicate the stereochemistry of substituents on asymmetric centers, where applicable. Ignore any inorganic byproducts. 1118 & CH3OH heat Draw One of the Major Products Draw One of the Major Products Draw One of the Major Products3. Draw the mechanism for the following elimination reaction. Be sure to clearly show the configuration of the substrate during elimination and the stereochemistry of the final product. Ph Br F Bri H NaOCH₂ HOCH, NaOCH, HOCH,5 Draw all products of the following reaction and show the mechanism by drawing the intermediate(s) that gets formed. Label the major and minor products and show the stereochemistry if applicable. Br. CH3OH Heat
- A E OH OH H This is a(n) OH R B F PCC, CH₂Cl₂ H type reaction. The major product if R = CH₂CH3 is compound The major product if R = H is compound G Look at the given reaction and use the letter code corresponding to each compound in the blank to indicate the expected product(s), or fill in the blank with the appropriate vocabulary word or phrase. If a specific stereoisomer (e.g single enantiomer) is formed, select that isomer only. If a mixture of stereoisomers (e.g. racemic or diastereomers) is formed, select the single structure that shows the appropriate mixture (e.g. lines not dashes). If we convert the reagent to Na2CrO4, H₂SO4, H₂O: The major product if R = CH₂CH3 is compound The maior product if R = H is compound ??? OH D H H though compound10) Show the product of the following elimination reaction. You must also show both chair conformations (i.e., draw one and then ring flip to directly obtain the other conformation), and indicate the relevant conformation in which elimination occurs Br œ K'O rox.The given reaction scheme is an example of which type of reaction? O || R₁-C-OH + R₂-OH Oxidation Fischer esterification Nucleophilic substitution Reduction Rearrangement reaction Acid O || R₁-C-O-R₂ Meeting in "General"
- a Draw the structure of the intermediate (I) for the reaction below. Hg(O2CCH3)2 NaBH4 Product CH;OH H3C • Use the wedge/hash bond tools to indicate stereochemistry where it exists. If the reaction produces a racemic mixture, just drawv one stereoisomer.The reaction below is a base-catalyzed aldol reaction. O || CH₂-C-H CH3-C-H Ethanal (Acetaldehyde) H I CH3-C-H Ethanal (Acetaldehyde) NaOH Draw curved arrows to show the movement of electrons in the step of the mechanism shown below. Arrow-pushing Instructions AC⇒x= :O: || :CH₂-C-H OH Bl CH3-CH—CH2-CH -CH₂-1-1 a 3-Hydroxybutanal (B-hydroxyaldehyde; formed as a racemic mixture) :0: :0: || CH3—CH—CH2-C-H A tetrahedral carbonyl addition intermediate XR'R°CHOH-CR'R* R'R?C=CR*R* What should orientation of each substituent in reactant to convert it into product alkene? What is importance of their specific orientation?
