Question 11 (2 points) Which of the indicated protons in the following compound would appear most...
Question 43 (2 points) The reaction of 1,3-butadiene with hydrogen halide at 40°C will undergo addition under control O a) 1, 2; kinetic Ob) 1, 4; kinetic Oc) 1, 4; theromodynamic d) 1, 2; thermodynamic Question 44 (2 points) Provide the structure of the expected major organic product generated upon completion of the following reaction scheme: (CH3)3CCH2CH=CH2 HBO H₂O₂ H Br Br H (CHDECCHCH C (CH3),CCH2CH 11 Br Br ACCH.CH ICH, Section H (CH3)3CCH2CH-CH2 (CH3),CCHCH-CHE IV a) IV Ob) III...
Page 1 of 25 Question 1 (2 points) Which of the indicated protons in the following compound would appear most downfield in the TH NMR spectrum? III TV II O a) IV Ob) I OCI O d) III Question 2 (2 points) Identify one final major product in the following reaction sequence: CHO AICI, Ζη C.HNO c. H2SO4 CHE NH "NO NH NO M a) IV Ob) II OI Od)
Provide the structure of the expected major organic product generated upon completion of the following reaction scheme: (CH)ACCH_CALCEM (CH)ACCH, CILE (CH3)3CCH2CH-CH2 (CH3)3CCH2CH-CH2 HBr (CH3)3CCH2CH=CH2 H₂O₂ Н. Br (CH3)2CCH2CH-CH2 Br III II I Br HBr (CH3)3CCHCH-CH3 HW.CCHCI IV
5 points Save Answer QUESTION 6 Which of the indicated protons in the following compound would appear most downfield in the H NMR spectrum? TV O 1 QUESTION T 5 points Save Wsich of the folewing ntormationis primarily obinined trom intrared spectroscopy? Sch the web and Window
Which of the indicated protons in the compound shown below will appear the most downfield in the H NMR spectrum? D. IV How many signals would you expect in the H NMR spectrum of the compound shown below? A. 4 B. 5 C. 6 D. 7
Question 11 (2 points) Rank absorption of the indicated bonds in decreasing (highest to lowest) order of IR frequency H II Oa) III>II>I ob) >I>III Oc) III>I>11 od) 1>II>III Question 12 (2 points) Which of the indicated protons in the following compound would appear most downfield in the 'H NMR spectrum? IV Oa) IV ob) 11 Oc) od) III
Question 11 (2 points) Saved Rank absorption of the indicated bonds in decreasing (highest to lowest) order of IR frequency. II O a) III>II>1 Ob) 1>1>111 Oc) III>>11 d) />II>111 Question 12 (2 points) Which of the indicated protons in the following compound would appear most downfield in the 1H NMR spectrum? III IV II O a) IV Ob) 11 c)! O d) III
Question 9 (2 points) Identify the final product for the following reaction. 1. BH THE 2. O2, NaOH OH OH doy HII oa) IV ob) III OC) od) 11 Question 10 (2 points) Provide the structure of the expected major organic product generated upon completion of the following reaction scheme: (CH)CCH_CH=CH, HB HO H (CH)CCH.CH (снуусан,он- 1 Br (CH2jcChych do (touche con IV oa) IV ob) 11 oc) od) DI
Question 30 (2 points) What are the expected major products of the reaction sequence shown below? 1. 03 2. H20 e OH O=C=0 OH II III IV V O a) I and IV Ob) II, III and IV Oc) I and II O d) 1, III and IV Question 31 (2 points) A compound with a molecular formula of C10H1202 has the following 'H NMR spectrum. Which of the following structures is consistent with this spectrum? 2 o OCH2CH2CH3 0...
() 1. Which of the following alkyl holides would you expect to be most reactive in a unimolecular reaction? CH3 a) CsM , CH, CH, CH, Br b) CEHCH CH BY c) CH, CCH, Br d) CH, CH2 CH CHE сн. он сня Br e) CHICCHE CH3 (4). 2. What would you expect to be the chief organic product(s) when tert-butyl bromide reacts with sodium acetylide, i.e.. CH + - CH3-C-Br + Na CECH ? CH a) 1 b) II...