Consider this dissociation reaction. H ½ H One of the products of this reaction is methylamine. H H Using the curved arrow to guide your reasoning, draw the other product of this dissociation reaction.
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- Neat and clean please...3) Use the reaction shown below and the associated reaction energy diagram to answer the following questions. E A Но- + Br HO. Br- reaction coordinate a) In the space above, use curved arrows to show the mechanism of the reaction. b) Classify the reaction as either addition, elimination or substitution. c) In this reaction is hydroxide (HO-) acting as a nucleophile or as a base? c) Based on the reaction energy diagram, is the reaction endergonic or exergonic? d) Based on the reaction energy diagram, and assuming the reaction is reversible, would the equilibrium lie to the left or to the right? e) Which position on the reaction energy diagram (A, B or C) corresponds to the transition state?Explain why one reaction work and why one doesn't.
- draw the step one product and draw curved arrows to show the nucleophilic addition step.Why does Hammett Equation only apply to meta and para substituted rings and not others? ExplainA Moving to another question will save this response. Question 12 Identify the electrophile in a Friedel-Crafts alkylation (remember: the one that will react with the benzene ring) O aluminum tetrachloride ion O radical O carbocation O aluminum chloride O carbanion A Moving to another question will save this response.