paring For the SN 1 reaction, draw the major organic product, identify the nucleophile, substrate, and leaving group, and determine the rate limiting step. x Br H₂O (solvent) Draw the major organic product.
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- didentify the Allowry reactions, as substitution, elimination, or addition DrawWelection arrows to show how the in each reactors Circle and identify any reactive bands break & form intermediates of carbon. Ħ Br Br → AH-Br →→ → XB²3. Draw the reaction mechanism for the following reactions. When possible, label nucleophiles/electrophiles, carbocations, and oxonium ions. H* CI. a) H. + H2O + НОCHЗ H* OH H* H;C*** 4444 **** ***14 ****** 744444 250 ← → C 7 ✰ app.101edu.co Draw the major monobromination product of this reaction. 0 es Br2 (1 equiv) hv Draw Major Product C 1,502 JUN 30 Questio MacBook
- 1. OH ??? Br + B ОН For the above reaction identify the catalyst and reagents and also show the catalytic cycle.10. What is the major organic product generated in the reaction below? HO HO 40||!!!!!! (A) OH ...... (B) 1) 03 2) (CH3)2S HO O (C) H НО. (D)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.
- The order from most reactive to least reactive with aqueous ammonia is (А) CH--o-č-CH, * CH,--oCH,CH, * CH,--a CH--č-OCH,CH, ° CH,--c³ CH---o-č-CH, > CH3-C-OCH2CH3 | CH3-C-CI | (В) %3D > CH3-C-CI CH3-C-0-C-CH3 (C) > CH3-C-CI CH3-C-OCH2CH3 CH3-C-0-C-CH3 (D) || > CH3-C-CI CH3-C-0-C-CH3 CH3-C-OCH2CH35. (a) Draw the product/s of the reaction; (b) Indicate the mechanism: changed from acetone to methanol? CI CH3CO₂Na ; (c) What will happen if the solvent isOxidation reactions can be used in multistep syntheses to produce new functionalities for use in subsequent reactions. Consider the following multistep reaction when you draw the structures in Parts 1 and 2 below. Please explain mechanism's fore the products I and 2 но PCC 1. NaH > Product l Product 2 Br CH,C!, 2. Step 1 Step 2 HO
- b) Identify A and B and provide mechanism of the reaction. NH2 HONO heat A `CO2H H;CO,CWhich of the following species has the most stoble anion? Consider the free energy profile for the transformation A to 0 ye on Dut of me overot reoction is endergonic andoemic evergone Refer to the following reaction mechanism slow CH, C-OCH fast CH-C OCH, OH CH,0 OH fast CH,C-O CH,OH The least stoble transition staote has which structure 8- A. CH-C-OCH3 B. CH, C OCH, C. CH, C-OCH, D. CH, C,OCH OH OHIdentify the major product of the reaction of an alkyne shown below. | ||| OH 1. Hg(OAc)2, H2O 2. NaBH4, NaOH ОН || IV 。 。 H