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- Please 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.Why does Hammett Equation only apply to meta and para substituted rings and not others? ExplainGiven what's provided, what product forms?
- Give a clear explanation handwritten answer..complete the following reaction with explanationOchem... What is the major product for the following three-step reaction sequence? Also, provide the structures for the major organic products formed in each step. See attached imageIn base-catalyzed halogenation of acetone, the second (and third) on the same carbon. How do you explain why while halogenation takes place, it does not occur on the carbon in the other methyl group?
- please answer entirely with detail Question 1 What arenium intermediates are formed in the ortho- and meta-substituted products of the following reaction? Draw a mechanism that leads to the formation of each intermediate, and use resonance structures to explain which would be the major product. CH :Br: ?I cannot figure out this question about ozonolysis of an alkene? There are two double carbon bonds to choose from on the ring, so how do we know what is being acted on? (if that makes sense) Thank you!Help! Please explain in detail. Thank you! Avobenzone is an active component in many sunscreens. It can exist in an equilibrium between its keto and enol forms. The enol from of avobenzone is given below. (A) Draw the keto form of this compound (B) Which tautomer (keto or enol) exists in a higher equilibrium percentage? Explain your reasoning.
- 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.In base-catalyzed halogenation of acetone, the second (and third) on the same carbon How can we explain why the halogenation does not occur on the carbon in the other methyl group? explain?All this worksheet asks for are the major substitution products and the major elimination products, please help me!