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Please answer question 2 I already have question one. Thank you so much!
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- Name the structure. Heating compound A in the presence of H2SO4 results in which product?Provide the structure of the major organic product of the following reaction and? explain the stereochemistry which results in this product. 2-Pentanol reacting with 1.) PBr3, pyridine 2.) NaCNProvide the products, intermediates, and/or reagents forthe following reactions:
- Provide a mechanism for the following isomerization in aqueous acid. Thank you in advance!Give the reactants and the mechanism to synthesize the following:draw a dehydration reaction and provide a detailed mechanism, explaining the formation of all possible products using appropriate chemical terminology.
- Tautomerization is a process in which an enol yields a ketone Give one examplefor a keto to enol tautomerization. Which form is more stable. Also, which ismore stable the E isomer or the Z isomer of 2-Chloro, 2-Butenegive the mechanism of the following reactions and explain why any selectivities occur.When 1,4-dibromobutane was treated with excess ethanamine at propanone, the main product had the molecular formula C6H13N. Deduce the structure of this product by proposing a mechanism for the reaction.