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 > Q Dr
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- 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. NaSH THF Q Tap here for additional resources2. Complete the following: Stereochemistry and regiochemistry may be important. type a) NaOH (aq) b) neutralize ➤ OMe a) LiAlH4, ether NMe2 f) b) H3O+ type b) a) HS SH ZnCl2, H+ b) Raney Ni g) type formation of thioacetal/desulfurization HO type Hell-Volhard-Zelinsky Reaction h) CO₂Et type Wittig Reaction H H₂N OEt OH DCC, CH2Cl2 Ph type a) NaH, THF CO₂Et d) b) BnBr, THE CO₂Et c) NaOH(aq); HCl(aq); heat type type HO type (COCI)2, cat DMF CH2Cl2 j) CI type a) NHEN b) LiAlH, THE c) H3O+ CO₂Me CO₂MeD. Question. When a-pinene is boiled in dilute aqueous acid, the following reaction occurs. Propose a complete mechanism and label the C atoms in the product to correspond with those given in the reactant. Identify the chiral center in the product and explain exactly how the product is formed as a racemic mixture. Include non-bonded electrons and formal charges. H #30 H H₂O, heat a HI!!! f H a-pinene b (rac) ܝܐ OH
- Use 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 SupportO (1) H20, H*; (2) Jones reagent (1) H20, H*; (2) PCC, CH2CI2 (1) conc. H2SO4: (2) Jones reagent O (1) H20, H*; (2) Tollens reagent (1) conc. H2SO4: (2) PCC, CH2CI2 O (1) conc. H2SO4: (2) Tollens reagentBuild a model of methylcyclohexane, and use the model to complete the following Newmanprojections of methylcyclohexane in the chair conformation: a. When the methyl group is in an axial or equatorial (circle one) position, the molecule is inits lowest potential energy conformation. b. Label one Newman projection above anti and the other gauche to describe the relationshipbetween the methyl group and C3 of the ring. c. In general, which is a lower PE conformation, anti or gauche? d. Explain how your answer to b and c provide an explanation for why it is more favorable fora large group to be in an equatorial than an axial position.
- Provide the major product of the reaction sequence. If cis/trans isomers are possible, draw only the major isomer. If enantiomers are possible, do not specify configuration. Select Draw Rings More Erase // H 1) Br2, heat 2) 2 equiv. NaCN DMFPart A || CH2=CH' CH3 Draw the molecules on the canvas by choosing buttons from the Tools (for bonds), Atoms, and Advanced Template toolbars. The single bond is active by default. Show the appropriate stereochemistry by choosing the dashed or wedged buttons and then clicking a bond on the canvas. EXP. CONT. H +) C CI Br Marvin JS [1] by O ChemAxon F P.Draw the product of the reaction shown below. Use a dash or wedge bond to indicate stereochemistry of substituents on asymmetric centers, Ignore inorganic byproducts. D At a Draw Drawing
- This is a stereochemistry consideration –how the atoms add with regard to space (R/Sand E/Z).what is degree unstaturation of the following ? and draw 2 structures per each numberWhat reagents are appropriate to carry out the conversion shown? - OH LOM 1. mCPBA; 2. CH3MgBr; 3. H₂O O 1. CH3MgBr; 2. H₂O O 1. mCPBA; 2. H₂O O mCPBA + enantiomer