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- Explain why pentane-2,4-dione forms two different alkylation products (A or B) when the number of equivalents of base is increased from one to two.Draw the structures of all possible products formed from the following reaction. Specifiy the type of substitution or elimination pathway. Demonstate the stereochemical outcomes of the reaction by drawing your products in wedge dash form when necessary.For the following reaction, use the identity of the alkyl halide and nucleophile to determine which substitution mechanism occurs. Then determine which solvent affords the faster reaction.
- 6) Develop a series of reactions we have covered in lecture that would produce the following molecules. Use any reagents necessary, but you must start with an alkene with one double bond (any alkene you choose) as one of your reactants. онBy taking into account electronegativity differences, draw the products formed by heterolysis of the carbon–heteroatom bond in each molecule. Classify the organic reactive intermediate as a carbocation or a carbanion.Draw the major organic substitution product or products for (2R,3S)-2-bromo-3-methylpentane reacting with the given nucleophile. Clearly drawn the stereochemistry, including a wedged bond, a dashed bond and two in-plane bonds at each stereogenic center. Omit any byproducts. Draw the major organic product or products.
- To synthesize the following substances using any alkene as a starting material. Name the starting material.A mechanism pattern involved in this reaction is loss of a leaving group rearrangement nucleophilic attack substitutionExplain why pentane-2,4-dione forms two different alkylation products (Aor B) when the number of equivalents of base is increased from one totwo.
- Given the organic product form in each of the following reactions draw a 3-D representation for the product molecule showing its correct configuration. Explain why pentane-2,4-dione forms two alkylation products (A and B) when the number ofequivalents of base is increased from one to two.In organic chemistry, an elimination process involves the removal of the hydrogen and a halide (i.e. dehydrohalogenation), in which they are ___ to each other, forming an alkene. syn-orientation co-periplanar anti-periplanar Z- orientation