i he diagram below shows two synthetic pathways by which the compound W might be prepared. C3H,OH C2H5OH [0] P [o] S Q C3HGO2 T CH4O Cl2 U.V.V R C3H5O2CI V C3H5ON V W CH;CH(OH)CO,H Standing over concentrated H2SO4

Q: Predict the major product for the reaction shown. excess CI CH,CH2CI 1. KMnOд/NaOH/н-0 AICI3 AICI3…

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Q: What Is the product of the followlng reactlon? HO OH

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Q: CH3NHCH3

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Q: (d) Propose a reaction mechanism to account for the following reaction. AICI3

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Q: CH3 CH3 CH3 CH,CH,CH2 CH3 CH,CHCCH, CH,CCHCH3 CH3CH2CH,CHCH2 ČH3 CH3 ČH3 ČH3 :

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Q: Which of these gives mostly the meta product when treated with Br2 / * ?Fe a. b. HN d. O-CH,

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Q: ) Propose a mechanism for the substitution reaction in Step 2.

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Q: What is the predicted product of the reaction shown? NH3 O,N- O2N- -NH2 II O2N- CI O2N NH2 IV O2N-…

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Q: Mg Et,0 CI CO2 then H+ A В + D HN С.

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Q: b. Provide mechanisms and/or products for the following transformations. Po Ln, Cul, PhBr 1. HBpin,…

A: Note : 1-hexyne reation with HBpin followed by PdLn is called Suzuki Miyura coupling. 1-hexyne…

Q: Predict the major product of the reaction K½Cr,O7 HO, H2SO4

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Q: Provide the structure of the product(s) with stereochemisty if appropriate. If multiple products…

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Q: II. Predict the products of the ff: elimination reactions and show the mechanisms involve. (a) HO…

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Q: . Provide the major organic product of the reaction below: Brz hv Br Br Br None A. 36. What is the…

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A: See major products below.

Q: 42 Give the reagents and reaction conditions for the conversion of I to li A) SOCI, at room…

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Q: Correct order of reactivity of following compounds towards Grignard reagent. HO CI (1) ÑO, (II) a.…

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Q: CH,COCI AICI3 NH2NH2 KOt-Bu DMSO MeO. MeO Et MeO Me А B `NH2 MeO. MeO. `Et CI C D

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Q: HBr А NaCN B HCI/H20 C SOCI, D. E H2O2

A: When alkene reacts with alkyl halide in presence of H2O2 , it follow anti-markovnikov's rule.

Q: 2.11 Account for the increase in the ratio of 1-alkene to 2-alkene products as the base is changed…

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Q: Ph,CuLi NO 2 OMe 1. nBuLi 2. PHCHO OMe 1. nBuLi 2. PHCHO Br Br LOME | Pd(PPH3)4

A: The details solution for this reaction is provided below in attach image.

Q: 21. Provide all possible E2 products with the correct stereochemistry. Label the major elimination…

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Q: d) Brg, FeBra e) F. Ph. Ph AICla IZ

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Q: 6. Provide the missing reagent(s) that gives the desired product in high yield. RCH-CH₂96m2-5r DOH H…

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Q: 3 KMNO4 H3o* _NH2 4 +

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Q: II. Predict the products of the ff: elimination reactions and show the mechanisms involv HO H2SO4…

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Q: 1) E PB13 Mg, ether 2)H3O* OH F G 1) Co H2CrO4 2)H3O* E

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Q: b. Provide mechanisms and/or products for the following transformations. Pd°Ln, Cul, PhBr 1. HBpin,…

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Q: Provide the expected major organic product of the reaction sequence shown. 03 - IV and V O V only II…

A: This reaction is known as reductive ozonolysis. Let us discuss its mechanism to find out the answer.…

Q: но осн 1. b. CI CI H DMSO HO, 2. NET3 C. of PPH3

A: Hemiacetal deprotection Swern oxidation Wittig reaction

Q: 5.9. Suggest mechanisms that account for the outcome of the following reactions: а. Si(CH3)3 1) Br2,…

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Q: OH 1) ТBDMSCI 2) а. NaCCCHg b. Hзо* H,C 3) H2. Pd/C 4) BUANF, THE

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Stereochemistry and Isomerism

Stereochemistry deals with the three-dimensional structure and properties of molecules. It explains the arrangement of atoms and their manipulation within a molecule in a 3D structure. Stereochemistry can be dealt with all types of molecules. Based on the stereochemistry of a molecule, the physical and chemical properties of the molecules vary.