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- The conversion of 3 alcohols into alkenes under acidic conditions involves two cationic intermediates. For each reaction, draw the complete mechanism using curved arrows.Identify A–F in the following reactions.A hydrocarbon of unknown structure has the formula C8H10. On catalytic hydrogenation over the Lindlar catalyst, 1 equivalent of Η2 is absorbed. On hydrogenation overa palladium catalyst, 3 equivalents of Η2 are absorbed. (a) How many degrees of unsaturation are present in the unknown structure? (b) How many triple bonds are Present? (c) How many double bonds are present? (d) How many rings are present? (e) Draw a structure that fits the data.
- Please answer ASAP Draw the arrow-pushing mechanism for the following reaction. 1) P(OCH2CH3)3, NaH 2) 4-Methyl-2-PentanoneDraw the major product formed when HBr reacts with the following epoxide. Use wedge/dash bonds, including H's at each stereogenic center, to show the stereochemistry of the product.Axial alcohols are oxidized faster than equatorial alcohols by PCC and other Cr6+ oxidants. Which OH group in each compound is oxidized faster?
- Identify the correct ranking of the following molecules from most prone to nucleophilic attack at a sp^2 carbon to least. The correct answer is D, but please explain.Draw the products formed (including stereoisomers) when each compound is reduced with NaBH4 in CH3OH.Draw a stepwise mechanism for the following reaction that illustrates how two substitution products are formed. Explain why 1-bromohex-2-ene reacts rapidly with a weak nucleophile (CH3OH) under SN1 reaction conditions, even though it is a 1° alkyl halide.
- Draw a stepwise mechanism for the attached reaction that illustrateshow two substitution products are formed. Explain why 1-bromohex-2-ene reacts rapidly with a weak nucleophile (CH3OH) under SN1 reactionconditions, even though it is a 1 ° alkyl halide.Draw the products formed when A or B is treated with fo following agent. In some cases, no reaction occurs. [1] CH3MgBr (excess); [2] H2OFor alkenes A, B, C, and D: (a) Rank A—D in order of increasing heat of hydrogenation; (b) rank A—D in order of increasing rate of reaction with H2, Pd-C; (c) draw the products formed when each alkene is treated with ozone, followed by Zn, H2O.