QUESTION 3 Which of the following haloalkanes would not undergo the reaction below? R-X + CH3S...
11 TEW 9:20 PM 19%D4 х Question H7.36 - Level 2 Unanswered Which of the following haloalkanes would not undergo the following reaction? R-X+ CH30-- CH3OR +X A (CH3CH2)2CHI CH3C1 (CH3 CH2)3COSO2CH3 CH3CH2I CH3CH2CH2Br Unanswered Submit
please help. Question 7 3 pts Which of the following compounds will undergo an SN2 reaction most readily? (CH3)2CHCH2CH2CH2F (CH3)3CCH21 (CH3)2CHCH2CH2CH21 (CH3)2CHI
please explain why 17. Which of the following compounds will undergo an SN2 reaction most readily? (CH3)3CBr, (CH3)2CHI, (CH3)2CHCH2CH2CH2Cl, (CH3)2CHCH2CH-CH21 メー 1 E2 18. Provide the structure of the major organic product which results when (S)-2-iodopent treated with NaCN in DMSO.
which of the alcohols below would you predict to undergo please help 12. Which of the following is/are the major product(s) of reaction below cH3 HO HT 13. The acid catalyzed dehydration of the alcohol below gives a major product which results from a carbocation rearrangement. Identify the major product. #2504) heat 3 cu CH2CH 14. What is the intermediate in the following reaction? + Brz cHack d) 15. a) b) c) d) The hydrohalogenation reaction can be described as:...
QUESTION 1 QUESTION 2 QUESTION 3 Which of the following compounds undergo reduction with H2/Pt? A. CH3(CH2)3COCH3 B. CH3(CH2)3CHO C. CH3(CH2)3CH2OH D. A and B E. all of the above
Which of the following alkyl bromides would undergo a relatively fast E2-type elimination reaction? Br Br A) B) C) D) oc "A dd Br Br А с
Which haloalkane shown below would be expected to react the fastest in a typical SN2 reaction? CH, 1-CH CH, CH -C—C=CHC1-C-CH3 н CH CH (b) CH3C1 CH; CH; Br—C—C=CH H CH; (e) CH; I-C-C=CH H H CHI (f) a. a b.b 10cc d. d e.e f. f
6. Which of the following carbocations would NOT be likely to undergo rearrangement? A) CH3CHCHCH3 CH3 CH3 B) CH3CHOCH3 CH3 CH C) CH3CCH2 CH3 D) CH3 CH3CHCH2 E) CH3 CH3CCHCH2CH3 CH3 7. Which alcohol would initially produce the most stable carbocation when treated with concentrated H2SO4? A) CH3 CH3CCH2 CH3 он CH3 B) CH3CHCHCH3 он CH3 C) CH3CHCH2CH2OH CH3 D) HOCH2 CHCH2CH3 E) CH2 OH CH3CHCH2CH3 Page 4
3. Which one of the following alkyl halides would react faster by unimolecular nucleophilic substitution (SN1)? PhCH2C1 Phci Ph2CHCI CH3C1 (CH3)2CHCI A B С D E 4. Which one of the following compounds is optically active (chiral). A B С D E
A26 Choose which of the following reactions would NOT proceed as written: OH + CH3S SCH, + OH OH + PBrz - → 3 . Br + H₃PO3 HI MeOH OH CN + NaCN NaCl OH (A) I only (B) I and III only (C) Il only (D) IV only (E) II and III only