- Complete the following reduction reactions, Draw the structure of the product. Name th reactant and product. a) CHy-CH-Ç=o Ni + Hy - It CH3 b) o-と-CH--CHg + Hy Ni Ni c) CHy-CH-CHy + Hz CHz と=o CH3 d) CH3 Ni + H,
Q: Draw the products in each reaction. CH,CH3 CH;CH,OH K* -OC(CH,)3 а. Он CH3CH2O b. CH3-C-CH,CH3 d. CI
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Q: Zn/ Alcohol (C), CH, – CH-CH, Br Product (C) formed in this reaction is Br
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Q: show the synthetic scheme to achive a final product L R-C-0-0-4 !! OH он 4 DR. CO₂ H 2) H₂ot Ⓒ
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Q: Select all the possible reducing sugarls from the list below. сно H- CH2OH CH2OH он HO- он онн но-…
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Q: HO (i) (R)-2-bromobutane 25 C 25"C ) ()-3-Bromo-3-methylhexane MeOH (k) (5)-2-Bromooctane MeOH, 60°C
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Q: Complete the following reactions CH3 a. CH3-CH-O-CH,CH3 + HI CHO b. NaBH4 COOH
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Q: Complete the following reactions: || C-0-CH,CH, +NAOH- a. b. CH;(CH,),-C-0-CHCH,+H,O CH3
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Q: 1- Benzene + HNO, ----- H;SO - 2- Iso-butane + CL,-- 250 - 400C - and 3- Propyne + Brz- + Brz 4-…
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A: Since you have posted a question with multiple sub-parts, we will solve first three subparts for…
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- Answer the following questions involving organic synthesis: c.) Write a reasonable forward synthesis for the conversion of 2-bromopentane to ethyl methyl ether. d.) Write any reaction with an alkene that occurs via a syn addition and draw its transition state. e.) Write any reaction with an alkene that occurs via an anti addition and draw its transition state. f.) Define Markovnikov’s rule and write out two reactions: one that is a Markovnikov addition and another that is an anti-Markovnikov pathway.Fill in any starting materials, reagents, or products to complete the reaction.What product is formed when D-Gulose is treated with a. CH3I, Ag2O b. The product in (a), then H3O+ c. The product in (b), then C6H5CH2Cl, Ag2O
- 1. Propose the complete reaction mechanism and reagents used for the production of hexan-2-olfrom hex-1-ene. Name the reagents, intermediate and final product/s formed.When toluene is treated with sulfuric and nitric acids under special conditions, three nitro (NO2) groups are substituted for hydrogens at the 2, 4 and 6 positions on the ring (the next section discusses why the 2, 4, and 6 positions are substituted). The product is a highly explosive substance called 2,4,6-trinitrotoluene. This subastance is commonly known by a three letter name. What is it?Ignoring E and Z isomers, what two enols are formed when pent-2-yne is treated with H2O, H2SO4, and HgSO4? Draw the ketones formed from these enols after tautomerization.
- 4. WHAT ARE IMINES? HOW ARE THEY FORMED? 5. WHAT IS GRIGNARD REACTION? WHAT CONSTITUTES A GRIGNARD REAGENT? 6. WHAT IS KETO-ENOL TAUTOMERIZATION?What starting material is needed to synthesize each compound by a ring-closing metathesis reaction?What alkene can be used to prepare each alcohol as the exclusive product of a two-step hydroboration–oxidation sequence?
- Classify the reaction type. a. oxidation (Benedict's) b. reduction (hydrogenation) c. acetal formation d. hemiacetal hydrolysis e. acetal hydrolysis f. mutarotation g. hemiacetal formationDraw the product formed when (CH3)2CHOH is treated with following reagent. SOCl2, pyridineA. Complete the reactions by adding in the correct reagents & starting materials. Please refrain from using H2 reductions/PCC oxidation.