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- Draw the appropriate curved arrows and products for each set of reactants undergoing a coordination step. Identify each reactant species as a nucleophile or electrophile. (a) NH₂ + AICI, →? (b) H₂O + BF₂? (c) ³0° H₂C OH - >?n17 of 17 > Draw curved arrows to depict the formation of the keto form of an enolate ion via a strong base, represented by B. Complete the resonance structures of the enolate anion's keto and enolate forms with bonds, charges, and nonbonding electron pairs. Use curved arrows to show how the keto form resonates to the enolate form. Step 1: Add curved arrows to show the formation Step 2: Complete the resonance structure of the of the keto form. keto form, then add curved arrows. Select Draw Rings More Erase Select Draw Rings More Erase CHO C H : B BH MacBook Pro G Search or type URL & # $ 9. %3D 3 4 6 7 8 { Y U P. E R T J . D F ? C V В N M + I| .. ..Q12) Which of the following reaction generates carbocation intermediate? (A) E1 (B) E2 (C) both E1 and E2 (D) Neither E1 or E2 Q13) (True/False) The reaction undergoes with E2 mechanism over Sn2 mechanism when tertiary carbon was used as electrophile. (A) Statement is True (B) Statement is False (C) Statement can be true sometimes (D) I have no idea but I will ask my mother
- Consider the taollowing transtormation to answer the 3-part question. "Br OH CI 2 i) Can substrate 1 undergo intramolecular SN2 reaction? | Select] ii) Can substrate 2 undergo intramolecular SN2 reaction? [ Select ] iii) Can substrate 3 undergo intramolecular SN2 reaction? ( Select )29) Draw the curved arrow mechanism, key intermediate, and product with the correct Stereochemistry for the following reaction Br2, H20Draw Intermediate CH3OH₂+ protonation H H3C -0 H Q CH3OH deprotonation loss of H₂O elimination H3C :0 ÖH -CH3 Draw Intermediate CH3OH deprotonatio Please select a drawing or reag
- Q6) (True/False) Unlike SN1 reaction, a nature of leaving group is not very important for E1 reaction. (A) Statement is True (B) Statement is False (C) Statement can be true sometimes (D) I have no idea but I will ask my motherCurved arrows in reaction (a) in this mechanisms is incorrectly written. Correct it. (a)-(d). oH-OH, он он OH Me OEt Me OEt Me Me OEt * OH, OH OH2 (b) (a) (c) OH2 EIOH + H,0* Me OH Me HO. (d)What is the mechanism for the following reaction?
- 1) Draw a plausible mechanism on the next page for the following reaction by using the guidelines, the template, and the instructions below. 요 HO OH [H₂SO4] -H₂OIdentify the best conditions to complete the SN2 reaction shown below. A) CH3I, THF B) CH3CH₂I, THE C) CH3CH₂CCNa, THF D) CH3CH₂CCNA, CH3OH E) KI, THF4. Which arrow identifies the nucleophilic site in the molecule shown? <40 a d