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- Propose a structure for the product with formula C9H17N that results when 2-(2-cyanoethyl)cyclohexanone is reduced catalytically.M8. draw the products formed in the following transformations A-CSelect the necessary reagent(s) for the following transformation. a. I2 b. H2/Pt c. Cu^2+ d. H+/H2O e. NaOH f. K2Cr2O7
- Choose the best reagents to complete the following reaction. There's another answer choice not shown on screen: E) 1. CH3Li 2. H3O+ Hint: The correct answer is not option C.The reaction of (S)-2-bromopentane with potassium cyanide to yield 2-methylpentanenitrile (2-cyanopentane) occurs via a nucleophilic substitution pathway. The reaction is 100% stereospecific.name the major product for the reaction of 4-methyl-1-pentyne with the following reagents ⦁ H2/Li or Na/NH3 (liq) at -78 degrees C
- Identify the product that can be obtained theoretically if the following reagents are mixed together: CH3CH2CH2CH2CH(OH)CH3 + PI3 5-Iodohexane Iodopentane 2-Iodohexane IodohexaneWhat products are obtained from the reaction of the following compound with H2CrO4 + Δ?Use the following choices for questions a-e: SN1 SN2 E1 E2 E1cb a. A polar aprotic solvent is preferred in this reaction. b. Product has an inverted stereochemistry. c-d. Proceeds in a concerted path. e. A mixture of products is obtained in this reaction.
- Show how Wittig reactions might be used to synthesize the following compounds. Ineach case, start with an alkyl halide and a ketone or an aldehyde.(a) Ph¬CH“C(CH3 )2Select the necessary reagent(s) for the following transformation.THERE MAY BE MORE THAN ONE a. I2 b. H2/Pt c. H+/H2O d. NaOH e. K2Cr2O7 f. Cu^2+Draw the favored product(s) of the following reactions (organic chemistry)