1 produt why? Julci Na CCH CH₃OH Slow why? CHI AC/ Nooche CH₂OH 2 produds fast...
KOIL E1OH Br H, CHi O LLiAIH 2 H,O H,C CH,CH-CHCH.CCH-CHi. CH,CH.OH- CH; HOCH-CH-CH-OH- CH,CH CHCH CCH CH CH, OH CH,CHCH,CH CH (acid catalyst) Clz HCl KOIL E1OH Br H, CHi O LLiAIH 2 H,O H,C CH,CH-CHCH.CCH-CHi. CH,CH.OH- CH; HOCH-CH-CH-OH- CH,CH CHCH CCH CH CH, OH CH,CHCH,CH CH (acid catalyst) Clz HCl
Make sure answer are correct thank you! Practice Questions 1. What reagents could CH CH CH.C-CCH 3. Which reaction would proceed the fastest? (A) CH,CH,OCHOH-- be used to accomplish the synthesis of this compound? CH3CH2OH + OCH3 CH CH OH SCH CH,CH2OH + N(CH3)h (B) CH3CH2Br + Na"で.CCH3 When 2-bromo-2-methylbutane is treated with a base, a mixture of 2-methyl-2-butene and 2-methyl-1-butene is produced. 2. CH,CH,OH+ OSC H4CH CHy 4. Which is a possible D Br CH3 H product of the...
5.41 Sterebenenlisuy acconug lo Camm g The reaction of 2,2-dimethyl-1-propanol [(CH),CCH OH], also known by the common name neopentyl alcohol, with HBr is very slow and gives 2-bromo-2-methylbutane as the major product. 5.41 HEг Br OH 65°C Give a mechanistic explanation for these observations. 5.42 (a) Assuming that the rate-determining elementary step in he rea tion of
age 7 19. The reaction of CH, CH, CCH, CH, with H,/Ni forms a. pentane. b. one particular chiral pentanol. c. an equimolecular mixture of two chiral pentanols . d. one achiral pentanol. e. no product. 20. The p-orbital of a methyl radical carbon, CH,, Contains how many electrons? a. 1 b. 2 e. 3 d. 4 e. 0 21. (2R, 35)-2,3-Dichlorobutane and (25, 3R) -2,3-dichlorobutane are: a. enantiomers b. diastereomers e. identical d. conformational isomers e. constitutional isomers 22....
predict the products of the following reactions 0 () CH,CH CCH,-C-OCH, NocCH (2) CH (3) Ho .heat (I) NaOCH2CH (2) H,O', heat (b) CH,-C-CH-C-OCH,CH,+ CH, (1) LDA -OH (c) Ph CH, () CH,CH,CH,Br (1) H2C-CH CH,Br (2) H0* OCH, NaOCH Ph (2) CH,CH,CH2CH2Br (g) product from part (f) (decarboxylation) 0 () CH,CH CCH,-C-OCH, NocCH (2) CH (3) Ho .heat (I) NaOCH2CH (2) H,O', heat (b) CH,-C-CH-C-OCH,CH,+ CH, (1) LDA -OH (c) Ph CH, () CH,CH,CH,Br (1) H2C-CH CH,Br (2) H0*...
2. In the following reaction, the nucleophile is 2H2O+CHI → CH3OH+I+H2O H2O. CHI. CH,OH. lodide ion. H30+. E.
predict the products 1 1) Na B Hy , CH₃OH 2) Ts Cl, pyridine 3) Na Et 4) Bra, H₂O 1) H₂O+ 2) Naz Cry Oy, H₂ SO4, H₂O 3) a Mgor 4) H₂O
3. Complete the following reactions. HBr conc. H2SO4 2-methyl-2-pentanol (CH)CO Na (CH3)COH РСС (1) BH3-THF (2) H2O2, OH ionard.
8. (2 points) Consider the mechanism below Step 1 (slow) A2 BC AB+AC AB BC B2AC Step 2 (fast) B2+ 2 AC overall A22 BC What is the rate law of the reaction? a. b. What compound is considered an intermediate?
Which statement about 2-methyl-1-propanol. (CH),CHCH,OH, and 1,3-propanediol, HOCH,CH,CH,OH is true? 2.Methyl-1-propanol is more soluble in water than 1.3-propanediol because 2-methyl-1-propanol has a smaller molecular mass. 2-Methyl-1-propanol is more soluble in water than 1,3-propanediol because 2-methyl-1-propanol forms fewer hydrogen bonds with water. O 1,3-Propanediol is more soluble in water than 2-methyl-l-propanol because 1,3-propanediol has a smaller molecular mass. O 1,3-Propanediol is more soluble in water than 2-methyl-l-propanol because 1,3-propanediol can form multiple hydrogen bonds with water Draw 2-methylpropanal. Include all hydrogen...