For the following acid-base reaction identify the correct curved arrow mechanism. 11 ||| IV V =H - |= II III OIV OV + Na NH3 + -H + CH + + H + ONH₂ e NH₂ NH₂ ONH₂ NH₂ Na + NH3
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- The following figure shows the energy profile of a nucleophilic substitution reaction. Potential energy :ÖH H HII.C H C-1 H HO--C---I HH Reaction coordinate H -CH HO–CHITH H + 1 According to this, it is correct to affirm: O The activation energy (4G°) shows that it is thermodynamically favorable. O Represents a reaction that occurs in one step where a pentavalent chemical species is formed. O The intermediate has lower energy than any transition state. O The formation of the intermediate releases energy and is therefore thermodynamically favourable.Draw the products of the reaction shown in the electron-pushing mechanism, including hydrogen atoms, charges, and nonbonding electrons. H3C-CH2 + :0H¯ ↑ Draw the products. Add charges and electrons where needed. Select 3 Draw |||||| Rings More с O Br H L Erase Q2 QFor the reaction shown below, circle the major product obtained when the | reaction is allowed to reach equilibrium. Place a box around the product that is formed the fastest. а H2C= CI H-CI CIH2C CIH,C H3C CI CI `CH3 H2C CIH,C H;C CI
- In each reaction box, place the best reagent and conditions from the list provided. 1) Br 2) 3) 4) DEET (the active ingredient in over the counter insect repellant) 5) Answer Bank Mg, Et,0 HN(CH, CH, ), (1 equiv.) H,O* CH,COOH CH,CH,NH, CH,CH, Br NH(CH,CH,),(2 cquiv.) НСООСH, H,CO НСООН CH, CH, OH NaCN NaNH, Br,, FeBr, SOCI, CO,Draw the mechanism for the reaction of an alkyl halide with sodium azide followed by reduction. Complete the mechanism of the initial step of the reaction, then identify the key intermediate and the product. Step 1: Draw curved arrows. o z + Na + || : z: I Step 2: Complete the intermediate. Na +List the rates of hydrolysis reactions of the compunds given below from large to small. Explain why H3C-Ö-NH2 i) H,C-č-cı H,C-č-OCH,
- 24. Which product is formed by the reaction ? A) | B) || C) ||| D) IV Br ОН NaH Br ... هستم IVWhich reagent is the nucleophile in the esterification reaction shown below? O || С-ОН Benzoic Acid methanol methyl benzoate benzoic acid sulfuric acid + CH₂-OH Methanol H₂SO - H₂O O || C-O-CH3 Methyl benzoate|| A A = B = C= Complete the reaction N-R My MH₂ NA PI-NH₂ G H ₂ OH S Puflux PI-NH₂ + B
- How many acid-base steps occur in this mechanism? :OH fö OH ₂ H CI: -H₂O (C5H12O) (CsH3O*) :CI: :CI:- yox (C5H1*) (C5H₁1CI)Mechanism: A reaction mechanism for the following reaction is shown below. H+ CEN CEN: N-H || -C-OH H₂O, H* Step 1 Step 3 N-H C-OH C=N-H H₂O Step2 .C=N-H H-O-H Semse anls a) The overall reaction is an example of b) Step 1 is c) Step 3 is d) Draw in the curved arrows for each step. e) Identify the nucleophiles and electrophiles where appropriate. f) Fill in the reaction energy diagram. C=N-H H₂O: rate determining step E个 reaction progress →What is the product of the following sequence of reactions? D | NaOH NaNH2 H3O+ || ||| explain each steps..explanation needed. don't give Handwritten answer IV NH₂