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- please 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) DDraw the major product of this reaction. Ignore inorganic byproducts. RCO3H Q Drawing Give detailed Solution, don't give Handwritten answerD Give a complete arrow-pushing mechanism for the following reactions. Show all important resonance structures of the intermediates and show exactly where each proton comes from and goes to. Indicate the Lewis acid and Lewis base (LA or LB) and whether they are also Bronsted acids and bases (BA or BB) for each intermolecular reaction. To preview image Click Here & EtOH HCI (cat.) O OEt OEt H₂O
- Complete the reaction scheme shown belowProblem 33 of 85 Submit Draw the missing organic structures or select the missing reagents in the following multistep synthesis. Ignore any inorganic byproducts formed. 1. NaOCH2 CH3 2. (CH3)2CHCI (1 equiv) Select to Draw 1. NaOC H2CH3 2. CH3Br (1 equiv) H3O+ Select to Select to Draw Draw heatQuestion 19 of 50 A) SN1 Consider the reaction below. Predict which reaction type is likely to occur. Submit CH3CCNa DMF Tap here or pull up for additional resources CI
- Provide the complete mechanism using curved arrow formalism for the reaction of p-isopropxlbenzoic acid undergoing nitration. Tell how many peaks in the 'H and 13C NMR spectrum that would be observed for the final product.With sulfides are treated with α,β-unsaturated ketones and aldehydes, they can attackeither through direct or conjugate addition. Based on the NMR spectrum obtained fromthe product of the reaction below, indicate whether the reaction occurs by direct orconjugate addition and provide an arrow pushing mechanismWhy is this synthesis incorrect??
