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- A H2N. Figure 9: Multi-step reaction sequenceIn Part 1 add the curved arrows to the nucleophilic acyl substitution reaction mechanism. In Part 2, answer the multiple-choice question about the reaction in Part 1. Part 1 See Periodic Table O See Hint :ö: :Br: Add the missing curved arrow notation. 20 F CI Br I Part 2 Which statement is most correct regarding the equilibrium for the above reaction? Choose one: O The equilibrium favors the right (i.e., Kea > 1) because acetate is a better leaving group than bromide. O The equilibrium favors the right (i.e., Keg > 1) because bromide is a better leaving group than acetate. O The equilibrium favors the left (i.e. Keg « 1) because acetate is a better leaving group than bromide. O The equilibrium favors the left (i.e., Keg« 1) because bromide is a better leaving group than acetate.6. Circle the structure with the most nucleophilic double bond. Put a box around the structure with the least nucleophilic double bond. OH
- Use the image below to answer the following three questions. Note: Subscripts are not shown in answer choices, ex: H2 should be H2, NH3 should be NH3. Product A Product B Product C a. The reagents that would selectively yield Product A are [Select] b. The reagents that would selectively yield Product B are [ Sclect] c. The reagents that would selectively yield Product C are [ Select]Circle the correct bolded word. a. Hydrogenation of an alkyne with palladium on carbon can / cannot be controlled to give an alkene. b. When a reaction becomes more exothermic, the transition state looks more like the substrate / product. C. Addition of two equivalents of HBr to an alkyne results in a vicinal / geminal dibromide. d. An SN2 reaction involves the collision of two alkyl halides to form a new carbon-carbon bond. True / False3. Does it matter what order you mix the reactants together in? If so, what is the correct order? 4. During the reaction, when do you start the timer? 5. How will you know when to stop the timer?
- Use the image below to answer the following three questions. Note: Subscripts are not shown in answer choices, ex: H2 should be H2, NH3 should be NH3. Product A Product B Product C a. The reagents that would selectively yield ProductA are [ Select] b. The reagents that would selectively yield Product B are [Select] c. The reagents that would selectively yield Product Care [Select]Same reaction as in Q1. H3PO4 What type of carbon does the nucleophile attack? O methyl O primary O secondary O tertiary O quaternaryWhich of the following is the rule which states that the more substituted product is the major product in an elimination reaction? O 1) Boyle's Law O 2) Markovnikov's Rule 3) Zaitsev's Rule O 4) LeChatlier's Principle
- Draw the most stable resonance form for the intermediate in the following electrophilic substitution reaction. _NH2 NH2 Br2 Br • You do not have to consider stereochemistry. • Include all valence lone pairs in your answer. • In cases where there is more than one answer, just draw one.4. Complete the phrases with one or more of the following terms: SNI, SN2, E1, E2. a) The reaction takes place in two or more steps. b) The reaction goes through a carbocation. c) The rate determining step has two reactants. d) The rate is independent of the concentration of nucleophile or base. e) Zaitsev's rule is often applicable to the products..For Sn1 and Sn2 reactions, explain why one type of carbon should react faster than others.