6. What would happen to the rate of the reaction below under the following conditions? (Use textbook for assistance. Circle the correct answer.) H₂O Хон a) Increasing the concentration of water? b) Decreasing the concentration of the halide? c) Changing the leaving group to bromine? d) Starting with 2-iodopropane? INCREASE SAME DECREASE INCREASE SAME DECREASE INCREASE SAME DECREASE INCREASE SAME DECREASE
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- 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. +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.Draw the reaction mechanism for the reaction between an aldehyde and water under acidic conditions. (H') H,0
- How is the rate of the reaction affected when concentrations of both nucleophile and alkyl halide are doubled for SN' reaction? (A) rate is doubled B) rate remains the same c) rate is tripled D rate is quadrupled(4 times)Tha fast answerplease answer both, will rate. 24) What is the product of the following reaction? C6H5CO₂Et + CH3CH₂CO₂Et A) CH,CCH₂CH₂COET 00 || B) CH,CCHCOÉt A) B) CH3 A) A O A) A B) B c)C. D) D 25) Which of the following is the conjugate base of ethyl butanoate? :0 B) B C) C 0 0 C) CH₂CH₂COCC6H5 (1) NaOCH₂CH3 (2) H₂0* 00 D) CH₂CHCOCC Hs CH3 C) D) el D) D
- Draw the FULL electron-pushing mechanism for the reaction to synthesise Lidocaine, including ALL intermediates (with formal charges) and electron pushing arrows. label the electrophile and nucleophile in each step!7. Predict the product and draw a complete curved arrow mechanism for the following reaction. 1) NaOMe 2x 2) HCI, H₂O6). What do you think would be the better nucleophile? Cu Organocopper reagent Cu Organocuprate reagent
- Can i see the mechanism for this reaction2. Mechanism Draw a complete arrow-pushing mechanism for the following reaction. CI AICI 3Complete the following reversible reaction and draw the mechanism of formation ofproducts. Indicate using the arrows of unequal length whether the shift in equilibrium will favor the reactants or the products. give 2 reasons