5. (5 points)Show how you would accomplish the following synthetic conversions. a. but-1-ene-butan-1-ol b. but-1-ene-butan-2-ol
U. Cis-nept-2-ene+CH212, Zn(Cu) 19. (10 points)Show how you would accomplish each of the following synthetic conversions. a. trans - but - 2 - ene + tra - 1,2-dimethylcyclopropane cyclopentene - cyclohexanol
LILULILULU U ULUULLOI CILI I ULIOL PUUDIO 3. (10 points)Show how you would accomplish the following synthetic conversions. (a). but-1-ene 1-bromobutane (b). but-1-ene 2-bromobutane ©. 2-methylbutan-2-ol2-bromo-3-methylbutane 4 (10 noints Predict the maior products 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...
what is the functional group of each of the following compounds butan-1-ol butan-2-ol butan-2-one propanal phenol
Show how you would accomplish the following synthetic conversion starting with ethanol as the only source of organic carbon atoms. You may use any necessary inorganic reagent and solvent. Show all reaction steps, reagents and conditions used. Extra Credit: There will be no partial credit. Answers must be correct. (10 pts) Show how you would accomplish the following synthetic conversion starting with ethanol as the only source of organic carbon atoms. You may use any necessary inorganic reagent and solvent....
Show how you would accomplish each of the following multistep conversions. Include all reagents and condtitions and show all reaction products. 4. Al Use conditions to selectively make the Z-alkene
3) Show how hex-1-yne might be converted to: a. 1-bromohex-1-ene b. 1,1,2,2-tetrabromohexane C. 2-bromohex-1-ene d. 2-bromohexane e. 2,2-dibromohexane 4) For each compound, give the product(s) expected from (1) HgSo./H2SO4-catalyzed hydration and (2) hydroboration-oxidation. a. hex-1-yne b. hex-2-yne c. hex-3-yne d. cyclodecyne 5) Predict the product(s) you would expect from treatment of each compound with (1) dilute, neutral KMnO, and (2) warm, basic KMnO, then dilute acid. a. hex-1-yne b. hex-2-yne c. hex-3-yne d. 2-methylhex-3-yne e. But-1-ene → butan-2-ol 6) Show...
Show how you would use simple chemical tests to distinguish between the following pairs of compounds. In each case, describe what you would do and what you would observe. a. butan-1-ol and butan-2-ol b. butan-2-ol and 2-methylbutan-2-ol c. cyclohexanol and cyclohexene d. cyclohexanol and cyclohexanone e. cyclohexanone and 1-methylcyclohexanol
(10 pts) Show how you would accomplish the following synthetic conversion starting with ethanol as the only source of organic carbon atoms. You may use any necessary inorganic reagent and solvent. Show all reaction steps, reagents and conditions used. OH ethanol 4-methylheptan-4-01
WOuld this be butan-1-ol or butan-2-ol? Help and explain please. 70 65 60 50 45 40 35 30 25 20 15 4000 3500 0 Type here to seach 11000 10000 9 A (s) 170.82 s) 31.89932 17 4000 2000 1000 -14000 13000 11000 10000 7000 A (h) 4.79 5000 2000 "1000 1000