Q2; Write the missing product; please write the mechanism of each step Fill in the boxes with correct structures. CH3CI AICI 3 This compound contains three rings. H+ KMnO4 AICI 3 A -H₂O
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- For the reaction below, draw he reachon mechanisms) (aurows) and predict al she major products. If no reachon will H2C acur brey explain whag: Br CH20HClear my choice Which of the following is/are the expected product/s of the reaction of 2-pentanone (CH3COCH CHACH) with excess Bro, followed by OHT? O CHCOCHBRCH,CH3 BICH,COCH2CH;CHa O CHBr + CH,CH,CH,COO OCHBR + CH,CH,CH,COOH Which compound can undergo Cannizzaro reaction? CH,CHO5. a) When the molecule below is treated with HCI, the product distribution shown is obtained. Use curved arrow formalism to draw a mechanism for this process. Account for the product distribution and draw resonance structures for the intermediate that leads to the major product. The m HCI CI + s 1o(29nil no awa eib ys leldwsio (2tniog 01).E (15 % CI2 tw ledsl< 1% lad olualom 85 %
- What is the predicted product of the reaction shown? ОТ O II O ||| O IV OV Н Na2Cr2O7/H2SO4/H2O IV || ОН ОН овог H V Ш OH ОНPredict the product(s) and provide the complete mechanism for each reaction below.Plastic photochromic sunglasses are based on the following reversible rearrangement of a dye inside the lenses that occurs when the lenses are exposed to sunlight. The original dye absorbs UV light but not visible light and is thus colorless, while the rearrangement product absorbs visible light and is thus darkened. (a) Show the mechanism of the rearrangement. (b) Why does the rearrangement product absorb at a longer wavelength (visible light) than the original dye (UV)?
- V. @Given the following mechanism fer me Y OCHS NaOH reaction show the detailed conversion of A to B •OCN3 CH3OH. OH (A) (B) c Ⓒ using the same detailed mechanism instead of cyclonexare ring as shown in product. B, propose and fer a product wil a cyclopentane ning instead of a cyclohexane viny. Ⓒ Exploumpand I with why campand (B) is preferred over the campanay campand with a cyclopentake ring..What starting materials are needed to synthesize each azo compounds O2N H2N- -N=N- CI но -N=N- -CH3 I0 Fill in the reagent or starting material needed or product in each reaction a) CgH;CH;CH;CH2Br CGH;CH;CH;CH¿NH2 b) C,H;CH;CH;CH2CONH, CH,CH;CH;CH;NH2 HCI P-CH;C,H4NH2 NANO2 P-CH;C,H&NH2 HCI/H;0 P-CH3C,H4NH2 CH;COCI4) Give the correct product with the correct stereochemistry. Me Me 5) Give the major product. hv HCI OC
- Propose a mechanism for this reaction. || » CH3COCH=CH, H,SO4 HC=CH + CH3COH H9SO4 Acetylene Acetic acid Vinyl acetate Vinyl acetate is the monomer for the production of poly(vinyl acetate), the major use of which is as an adhesive in the construction and packaging industry, but it is also used in the paint and coatings industry.Mechanism: A reaction mechanism for the following reaction is shown below. H+ CEN CEN: N-H || -C-OH H₂O, H* Step 1 wand woled mot ozsm E Step 3 N-H C-OH C=N-H Step2 C=N-H H-O-H H₂O motno vgiene fesrigid onlt to smotnos -C=N-H 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. H₂O: rate determining step to noipojovo hamwell sit 5(emise erit voittons 10) vanas mi sdgin al rainW di of E^ reaction progress →draw and explain the mechanism of this reaction OH CH₂ PhCOCI in py CH3 KOH in py 3 C OH H₂SO, in 0000 CH, CON