Part B CH3CH2 CH3 Br2 CH₂Cl₂ CH3CH2 CH2CH3 Draw the molecules on the canvas by choosing buttons from the Tools (for bonds), Atom appropriate stereochemistry by choosing the dashed or wedged buttons and then clickin HD EXP. CONT WV A ΔΟ H с N S H₂C Br CI CH3 Br C Br - H₂C- Од -CH3 P F
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- Can you assit with confirming product(s), define major/minor, show stereochemistry, if appropriate, and/or if no reaction occursThe AH° values of each compound is given below as kJ/mol. Calculate the entaphy change (AH) value of the following reacti on? 2CaOg) + 2SO2 (g + Ozg) →2 CasO41) -635.5 -296.9 0.0 -1432.7 (kJ/mol) A) 500.3 kJ B) -500.3 kJ С) -1000.6 kJ D) 2365.1 kJ E) -1094.1 kJPart A CH3CH2 CH3 C=C Br₂ CH2Cl2 CH3 CH2CH3 Draw the molecule on the canvas by choosing buttons from the Tools (for bonds), Atoms, and Ad appropriate stereochemistry by choosing the dashed or wedged buttons and then clicking a bon □ D C ® Q® H± 12D EXP. CONT. י • Α [1] Δ Submit Request Answer Marvin JS by Chemaxon H с N So о CI Br I P F
- Please help with part G, H, I, J::&:$:$;$$;$&:&What are the chemical structure of me сиз сиз (excess] following musing compocents Brz. mono substituted MAHAA 2 G3 77 excess KM 12 छाट reduction E2 Reduction (mild pond) NaBH3 CH 3 Mg Br HLOH H E3 HOW Hyle. bor. Holt aid. H3 oxymer/ demo. H2 Three compounds A, B, and C all have the formula C6H10. All three compounds rapidly decolorize bromine in CC14; all three are soluble in cold concentrated sulfuric acid. Compound A has an absorption in its IR spectrum at about 3300 cm, but compounds B and C do not. Compounds A and B both yield hexane when they are treated with excess hydrogen in the presence of a platinum catalyst. Under these conditions C absorbs only one molar equivalent of hydrogen and gives a product with the formula C6H12. When A is oxidized with hot basic potassium permanganate and the resulting solution acidified, the only organic product that can be isolated is CH3(CH2) 3CO₂H. Similar oxidation of B gives only CH3CH2CO₂H, and similar treatment of C gives only HO₂C(CH2)…
- Give the structures of A to E, showing the absolute stereochemistry in each case.Please help with part A, B, C, D:Complete the following: Stereochemistry, enantio-, and regioselectivity are important. CrO3, H2SO4 a) OH Bromination of an alcohol (Sn2) type EtO₂C CO₂Et b) b) d) H3CO type NH2 a) b) H3CO type a) b) OH g) type CN CI h) acetone Swern Oxidation type type CO₂H type Доно i) Me3SICI, Imidazole OSiMe3 Et3N, CH2Cl2 Br type a) Mg°, THF Br j) b); H3O+ H2SO4 (H+) MeOH OMe type type