Draw the product (constitutional isomer) that is formed when the reactant shown is treated with an excess of H2 in the presence of a palladium catalyst. Do not depict the configuration(s) of any stereogenic center(s). H₂ (excess) Pd Click and drag to start drawing a structure. show mechanism with explanation. don't give Ai generated solution C E O E 5 C

3) Complete the following: Stereochemistry and regiochemistry may be important. b) d) type type MeO Br type type type OH H Br E1 Reaction Borohydride Reduction H NaOAc DMF Асон HO PCC CH₂Cl2 H CO₂Et f) g) h) i) j) type type type type type OH OH Hydride Reduction MeHN Reductive Amination HO Br 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 Support

Identify compounds A–D in the following reaction sequence.

Give clear detailed Solution with explanation needed..don't give Handwritten answer

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Which would be the major isolated organic product of the reaction shown? O A OB OC OD OE H₂C H₂ A) A chiral alkene B) a meso compound C) a racemic mixture D) A chiral alkane H₂ catalytic Pt or Pd. E) a different product or a mixture of more than one of the choices in equal amounts

Give detailed mechanism Solution with explanation needed...don't give Handwritten answer

Draw curved arrows to show the movement of electrons in the step of the mechanism shown below. Arrow-pushing Instructions NOC XT :: [MgX]* H3C-C-0-CH3 CH₂CH₂CH3 :0: || H3C-C-CH₂CH₂CH3 + HạC—O: [MgX]* A ketone X

Please show full curved arrow mechanism for the reaction below, and include mechanisms for BOTH products. Will rate promotly.