question 4 please! b. BF3 +H20 d. NaNaphthalene e. H2S04 f. n-CaHgLi Consider the following monomers....
H2SO4 e. (CH3)3CBr + H20 → 4. In the following pair indicate which would be the most stable intermediate in a reaction and briefly explain your answer. [4 marks] CH3 CH3 CH CH3 Cc Home CH2 CHE H2C CH CH2 H3C a. CH - H₃C CH₂ H₃C CH₂ 5. Briefly explain the difference between substitution mechanisms SN, and SN2 and elimination mechanisms E, and E. [4 marks)
A. alkene B. alcohol C. aldehyde D. carboxylic acid E, ester F. ether G. alkyne 39. CH3-CH2-CH2-CH=0 39. 40. CH2-CH2-CH2-CH2-CH2-OH 40. 41. 41. CH3-CH2-CH2-C=0 OCH 42. CH3-CH2-CH2-O-CH2-CH3 42. 43. 43. CH3-CH2-CH2-C=0 OH 44. CH3-NH-CH2-CH2-CH3 44. 45. CH3-CH2-CH=CH-CH3 45.
26.) The general formula for a carbohydrate is: A) CnH2n+2 B) Cn(H20)n C) CnH2n D) Cn(H20) 27.) Which of the following functional groups comprises a carbon atom bonded to a hydroxyl group? A) Alcohol B) Thiol C) Carbonyl D) Ester 28.) A carbohydrate with 4 carbons is called a: A) hexose B) triose C) pentose D) tetrose 29.) A carbohydrate with 6 carbons and an aldehyde functional group is called a(n): A) ketohexose B) aldohexose C) ketopentose D) aldopentose A)...
5. Consider the following compounds: b) сH.CH.CH a) CH3(CH2)CH c) CeHsCCHy d) CHs(CH2)COH e) CHs(CH2) CH=CHCHs )CHs(CH2) CEN h) CHs(CH2) N(CHs) g) CeHsOH D CH-CH-CH,&N(CH,CH,сH,) i) C H5CH ) CH5(CH2)-COCH k) CH,CH2OH Which one(s) of the above would be soluble in water? Which one(s) would not be soluble in water but would be soluble in 5% HCI? Which one(s) would not be soluble in water but would be soluble in 5 % NaOH? Which one(s) would not be soluble in...
1) Name the following compounds, according to IUPAC rules: (20 pts.) a) b) CH3-CH2 CEC-CH-CH2-CH-CHs d) CH3 CH-CH-CH2-CH2-CH сH, CH3 e) CH3 CH3-C C-CH2-CH-CH2- CH3 f) CH3 -CH2-CH2-CH3 CH3-CH CH-CH-CH2 g) CH3 н - c-c CH-CH2-CH2 CH3 CH3 н i) -CHз CI Hас CH3-C CH2-CH3 CI j) CH2-CH3 "CH,—сн, CH2 CH3
e-g please e. 4-HC-C6H4-NH-C(O)-CH3 + Cl2/HC-COH H30* f. 4-nitro-1-chlorobenzene + NaOH ------> H20 g. Ph-CH2-CH2-CH2-CO2H + AICI: -------
QUESTION #10. WHY IS THE ANSWER B? MECHANISM PLEASE Tab Caps Lock 0. Which of the following compounds would NOT give a tert-butyl alcohol upon reaction with excess methylmagnesium bromide? 0 CI H3C 11. CH,CH,CH,CH,OH is the product (after acidic workup) of propylmagnesium bromide and 0 CH CH2 OH H C E SENT 12. The product of the following reaction is: CF FO list of d cn com (CH)2C C(CH3) CHCl,Koc(cHs)s A. 1,1-dichloro-2,2-dimethylpentane. B. 1,1-dimethylcyclopropane. C. 1,1-dichloro-2,2,3,3-tetramethylcyclopropane. D. 2,2-dichloro-3.3-dimethylbutane. not...
5. Consider the following compounds: a) CHs(CH2)eCH b) CH,CHE c) CeHs d сHысн,он e) CHs(CH2) CH=CHCH ) CH,Cна,саN g) CeHsOH h) CH3(CHa)N(CH)2 снHCH,CHNCHCHCнъ. i) CeHsCH CH5(CH)ncoCH k) CH3CH2OH Which one(s) of the above would be soluble in water? Which one(s) would not be soluble in water but would be soluble in 5 % HCI? Which one(s) would not be soluble in water but would be soluble in 5% NaOH? Which one(s) would not be soluble in water but would be...
CH3 но cCH2 CH2 H3C H3C-HC CH 2 CH3 CH-C он 14. Draw the following esters a) ethyl butanoate b) pentyl propanoate e) 2,3-dimethylpentyl ethanoate c) propyl 3-ethylhexanoate d) methyl 4-phenylpentanoatef) butyl 3-hydroxyheptanoate 15. Name the following esters CH CH3 H3 C) CH3 b) CH2 CH O-C--CH3 CH3 f CH2 d) CH3 но cCH2 CH2 H3C H3C-HC CH 2 CH3 CH-C он 14. Draw the following esters a) ethyl butanoate b) pentyl propanoate e) 2,3-dimethylpentyl ethanoate c) propyl 3-ethylhexanoate d)...
1) Name each of the following organic compounds: (a-b-c-e-f-g-j-k-I-m-n) a) CH3CH2CH2CH3 j) CH3CHBOCHBrCH3 b) CH3CH2CH2C(CH3)3 c) CH2=CHCH2CH2CH3 d) CH3CHCICH(CH3)2 k) CH2BrCH(CH3)CHCICH2CH3 1) CH2CH(OH)CH(CH3)2 m) (CH3)2CHCHO n) CH3CH2CH2COCH3 e) (CH3)2C(OH)CH2CH3 f) CH3CHO o) (CH3)2CHCOOH p) CH3CH2CN g) CH3CH2COCH2CH3 h) CH3CH2COOH 9) CH3CHBCH(OH)CH3 i) CH3CH(OH)CH2CHO r) CH3COCH(CH3)CHBCH3