Provide the complete mechanism using Curved Arrow Formalism for the reaction of 2-isopropylcyclopentanone treated with pyrrolidine in acid. If more than one product is generated state which is major and minor and explain why this is so. Include all resonance stabilized intermediates. Name the functional group generated.
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- Provide the complete mechanism using curved arrow formalism for the reaction of p-isopropxlbenzoic acid undergoing nitration. Tell how many peaks in the 'H and 13C NMR spectrum that would be observed for the final product.If possible please answer all questions. Provide a complete, detailed curved-arrow mechanism for the following reaction. Include all lone pairs and formal charges. Using the mechanism and a few words,explain the why the NaOH deprotonates at the a-position and not the b-position or the aldehyde hydrogen. Also explain why the indicated alkene is formed in the 2nd second rather than the other possible alkene product.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-Butene
- Give only typing answer with explanation and conclusion to all parts draw the mechanism for these 4 reactions with electron movement and arrows and products formed The dehydration of 2-butanol with H2SO4 The dehydration of 2-butanol with H2SO4 The dehydrobromination of 1-bromobutane with potassium tert-butoxide The dehydrobromination of 2-bromobutane with potassium tert-butoxideExplain the mechanism of the reaction oxidizing from cyclohexanol to cyclohexanone. Explain detailed.With sulfides are treated with α,β-unsaturated ketones and aldehydes, they can attackeither through direct or conjugate addition. Based on the NMR spectrum obtained fromthe product of the reaction below, indicate whether the reaction occurs by direct orconjugate addition and provide an arrow pushing mechanism
- Provide a reasonable mechanism for the following transformation. Includeall intermediates as well as arrows showing the making and breaking of bondsPlease provide a complete, detailed curved-arrow mechanism for the following reaction. Include ALL lone pairs and formal charges. Using the mechanism and a few words, explain why the NaOH deprotonates at the a-position and not the b-position or the aldehyde hydrogen. Also, explain why the indicated alkene is formed in the 2nd second rather than the other possible alkene product.Provide the curved-arrow mechanism to account for the following electrophilic aromatic substitution reaction. .CI Cl2 FeCl3
- Provide the complete mechanism using Curved Arrow Formalism for the reaction of (R)-3,3-dimethyl-2-hexanol treated with aqueous phosphoric acid. If more than one product is formed state which is major, minor, very minor, etc. Name the product(s).a) Write out the first 3 steps only(to the tetrahedral intermediate shown) in the 6-step arrow pushing mechanism showing how ethyl propanoate is hydrolyzed in acid to form propanoic acidand ethanol. b) NaOH/H2O also serveto hydrolyze an ester; briefly explain why NaOH/H2Ois generally preferable.Please don't provide handwritten solution... Give the major product and mechanism for the following reaction: