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- In 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.From the following reaction are step 1 and 2 correct?, explain why or why not and draw the whole mechanismochem help Predict the major product(s) for the following reaction sequence and provide the stepwise mechanism for both steps 1 and 2. see attached image
- 6. Explain why halogenation occurs twice in the following reaction. Ch₂ NaOH give both answer asap thanks 7. Draw a complete, detailed mechanism for the following reaction. Label the electron-rich and electron-poor sites in each step. H₂SO₂ OSOHOChem HELP need help with the following reaction scheme I'm not sure if step ii product or step iv product is correct... so please just show the mechanism for the entire reaction with products formed at each step. thank you!Predict the product of the reaction shown and complete the curved-arrow mechanism for its formation. (Hint: Friedal- Crafts alkylations can be used to form rings.) AICI, → a compound C,H2 + HCI PHCH,CH,CH,CH,CI- Step 1: Draw one curved arrow. Step 2: Complete the structure, then draw curved arrows for the EAS reaction. Select Draw Rings More Erase Select DrawRings More Erase H Al Cl H Al Cl : C : Al : d :
- 027 In 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 4 See Periodic Table O See Hint :0: :Br: Add the missing curved arrow notation. S CI Br 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., Kea > 1) because bromide is a better leaving group than acetate. O The equilibrium favors the left (i.e., Keq« 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. Determine whether each reaction occurs by an SN2, SN1, E1, and/or E2 reaction. Provide a detailed mechanism with curved arrows and the major product(s). CI NaSH DMF OMs NaOH H20, heat LDA Br DMF NaOH H20, heat OH HBr OH H*, H20 heat1. Draw the mechanism for the following reaction. Include all intermediates, formal charges, and arrows. ol CH3CH₂NH2 H*, -H₂O
- The given reaction takes place in acidic conditions under rigorous heating. Complete the reaction mechanism, adding missing atoms and lone pairs, charges, and curved arrows as necessary. Ignore hydrogen sulfate in steps 2 and 3. OH Step 1: Draw curved arrows. : он H₂SO4 A : 0: || OH : 11 Step 2: Draw a curved arrow. OH₂This reaction is an example of conjugate addition of a nucleophile to an a,ẞ-unsaturated carbonyl. O CH3CH2CH2CH=CHCSCOA H₂O OH CH3CH2CH2CHCH2CSCOA Draw the two resonance structures of the enolate anion intermediate for this reaction. • Draw an R1 group in place of COA. The R group tool is located in the charges and lone pairs drop-down menu. • Draw one structure per sketcher. Add additional sketchers using the drop-down menu in the bottom right corner. • Separate resonance structures using the symbol from the drop-down menu. ->> 90-87 O + ? ChemDoodle >I want maknaism for this reaction!?