10. (5 points)Predict the major products of the following reactions. a. cis-hex-2-ene+mCPBA in chloroform b. trans-hex-3-ene+peroxyacetic...
4.(10 points)Predict the major products of the following reactions. a. l-methylcyclohexene+aqueousHg(OAc)2 b. the product from part (a), treated with NaBH4 c. 4-chlorocycloheptene+Hg(OAC)2 in CH3OH d. the product from part (c), treated with NaBH4 5 5 nointsShow how you would accomplish the following synthetic ca
Predict the major products of the following reactions, and propose mechanisms to support your predictions ja) pent-l-ene HCI (b) 2-methylpropene + HCI c) l-methylcyclohexene + HI (d) 4-methylcyclohexene + HB Choose the correct X, Y, and Z for the following reaction? CH3-CH2-CH2-CH2-CH3 + XO2 → YCO2 + 2H20
Predict the major products of the following reactions. Include stereochemistry where applicable.(a) 1-methylcycloheptene + BH3 · THF, then H2O2, OH−(b) trans-4,4-dimethylpent-2-ene + BH3 · THF, then H2O2, OH−
1. Name this compound according to the IUPAC system, including stereochemistry (cis/trans, EIZ), if relevant. CIS-3- isopropyl Cyclopent-l-ene 3 2. Using the compound in #1 as the starting material for all these reactions, write in the products, including stereochemistry if relevant: HBr 1. Hg(OAC)2, H20 2. NaBH Br2 1. BH, 2. H2O2, OH Bra H2O Pd mcpba
predict the major products of the following reactions with appeopriate stereochemistry mCPBA lal H2O OH (b) H2SO4 EtOH zo (c) H2SO4 tor Br (d) 1) O₃ lel 2) DMS H₂ (f) PI HTML Editores BIU A- A - IX E 33 x X, TTT 12pt
9. (5 points) Elimination reactions of els NaOCHCH in ethanol can give the same or di or 3-methyleyelohexene (2). Which of (a)-(d) indicates the main products nation reactions of a 2-methylcyclohexanes with Ho in ethanol can give the same or different main product, 1-methylcyclohexene Br NaOCH, NaOCH CH,OH CH,OH trans cis a) 1 from both the cis and trans substrates b) 2 from both the cis and trans substrates c) from the cis, and 2 from the trans substrate d)...
please help 2. (5 points) Predict the products of the reactions of the following compounds with: 1. chromic acid or excess sodium hypochlorite with acetic acid. 2. PCC or NaOCl (1 equivalent) with TEMPO. a).cyclohexanol b).1-methylcyclohexanol c). cyclohexane d). 1-phenylpropan-1-ol 3. (6 points) Provide the major organic product of the following reactions.
Show how you would accomplish the following conversions a) trans-hex-3-ene to meso-hexane-3-4-diol. Please explain when to rotate. Thank you ! Show how you would accomplish the following conversions. trans-hex-3-ene to meso-hexane-3,4-diol . ~ CH,C01H HO Chocolate HO rotate CH,CO,H HO HO HO OH Submit Request Answer Part D trans-hex-3-ene to (0,2)-hexane-3,4-diol ~ Ho t do anemie van OSO. rotate racemic (d.1) HO Но он ~ rotate CH CO, HO CHCOM enten met racemic (d.1) HOOH CHICOH HO racemic (d.1) Но...
5. (3 points) Predict all the major products of the Balance the reactions. all the major products of the following electrophilic aromatic substitution reactions. HO, H,SO + HNO, SOH FeCl3 + Cl2 NO
1. Predict the major products formed in each of the following reactions, indicate if the reagent reacts either regioselectively or stereospecifically, or both in relevant cases (5 x 2-10 points): a. Write products of the reaction using Fischer projection. (2)-3-methyl-pent-2-ene - HCI 2 b. Write product/s of the reaction using Fischer projection. y Brze? c. Write product/s of the reaction using Fischer projection BH3 H2O2. NaOH 1 mole of Hz. Pd/C e. MeOH is in a large excess. Write products...