Which of the following compounds is MOST reactive with respect to an aromatic nitration reaction? Select one: O A. III OB. I O C. IV O D. II II Br III NO₂ IV C-H
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- II. Alcohols in Synthesis B.) How are alcohols used to make ethers in the Williamson ether synthesis? How do you design the synthesis of ethers using both acidic and basic Williamson ether synthesis strategies?The name for Reaction 1 is _____ while Reaction 2 is called _____. Choices: A. Williamson Ether synthesis, B. Hydration, C. Epoxidation, D. Acidic cleavage The reagent/s for REACTION 1 is/are ______ Choices: A. m-chloroperoxybenzoic acid, B. H2O/H3PO4, C. H3O+, D. HI The reagent/s for REACTION 2 is/are ______ Choices: A. m-chloroperoxybenzoic acid, B. water in acidic medium, C. dilute acid, D. hydroiodic acidWhich of the following statements about substituent effect in electrophilic aromatic substitution reactions (E.A.S.) is false? Electron-withdrawing groups (EWGs) passivates the benzene ring for ortho and para substitution Carbonyl group which are bonded directly to the ring are called electron withdrawing groups (EWGs) In nitration of benzaldehyde, major products are ortho and para-nitro benzaldehyde Regioselectivity in multiple subtitution is determined by the substituent which has a higher activation effect F, Cl, Br, and I are orto-para directing groups, but have passivating effect
- What is the best way to remeber the differences between Sn1, Sn2, E1 and E2 reations?Please provide 3 possible mechanisms for bromination of trans-cinnamic acid and pyridinium tribromide (Br2) with stereochemistry (wedge and dash bond) (1 for anti addition, 1 for syn addition, and 1 for 50:50 syn and anti additon).Do not give handwriting solution. please draw out what compound A is and then provide aroow pushing mechanism for thisreaction! thanks01 Cive the ctrientiono of Comnand 4 2.2 Provide a reasonable arrowpushing mechanism for the reaction in 2.1