Which of the following compounds would be most reactive to ring bromination? |
A) I B) II C) III D) IV E) V |
CH3 and NH2 are activating groups which activate the ring towards electrophilic aromatic substitution. But NH2 is strongly activating than CH3 group which means NH2 group strongly increases the reactivity of benzene ring towards electrophilic aromatic substitution.
CF3, Cl and NO2 are deactivating groups which deactivate the aromatic ring towards electrophilic aromatic substitution which means they decrease the reactivity of benzene ring to undergo electrophilic aromatic substitution.
Therefore, answer is option is E) V
Which of the following compounds would be most reactive to ring bromination? A) I B) II ...
3. Rank the following compounds in order of increasing rate of bromination from 1 to 5 (i.e., from 1 for least reactive to 5 for most reactive). ОН ОН ОН ОН ОН CH3 Br NO2 NO2 CH3 $ de represente en & NO2 - ii iv V iii iv 4. Which of the following compounds can probably be prepared in a good yield (as a major product) from benzene using two successive electrophilic substitution reactions? Check all that apply. Br...
7) Which of the following compounds would be least reactive toward electrophilic substitution? ofO2 to a) 1 b) II c) III d) IV e) v
H Mono-bromination of the following alkane, , (using Br, with ligbt) would give? Br Br Br Br Br IV V I II Select one or more: al b. 11 c. III d. IV De. V List the following compounds in order of increasing level of oxidation: LO II - III Select one or more: a. I, II, III b. III, II, 1 c. II, I, III d. III, 1, 11 e. I, III, II
Which of the following is most likely to be the first slop in the general mechanism for electrophilie substitution reactions? Arrange the following compounds in order of decreasing reactivity towards electrophilie aromatic substitution (most reactive first). V>II>I>III>IV II>V>III>I>IV IV>I>III>V>II III>II>I>IV>V IV>V>II>I>III Which one of the following substituents will not direct an incoming group to the ortho/para positions during electrophilic aromatic substitution? -CH_2CH_3 -CF_3 -OCH_3 -NHCH_3 -Br Which one of the following is not a resonance form of the cyclohexadienyl cation...
Which of the following compounds would show hydrogen bonding in their pure liquid state? i. HF ii. H2O iii. CH3OH iv. CH3NH2 v. (CH3)2NH vi. (CH3)3N vii. CH3OCH2CH3 Which of the following can form hydrogen bonds with methanol? i. HCOOH ii. NaOH iii. CH3NO2 iv. F- v. NH4Cl vi. benzene vii. CH4
Question 1 Which of the following hydrogens is the most acidic? II IV I III A. IV B. V C. III D.I E. II Question 2 What is the product, Z, of the following reaction sequence? iz H30+ T-H20)* ia. CI H307 + Z مل I II III IV A. IV B. II C. III D.V E.
Which of the following compounds would you expect to be antiaromatic? (i) cyclooctatetraene (ii) 1,3-cyclooctadiene (iii) cyclooctatetraenyl dianion (iv) 1-ethenylcyclooctatetraene (v) 1,3,5,7-octatetraene Select one: a. i only b. i, ii, iv and v only c. iii only d. i and iv only e. all the above From my working I found i, ii, iv, and v to be non aromatic and iii to be aromatic. Is non aromatic the same as antiaromatic?
Question 28 Which of the following compounds is most reactive towards a nucleophilic addition reaction? o e H Н H 1 11 IV II III IV V FO F10 FB F7 F6 F5 F4 F2 F3 * A & @ $ % 5 7 LO 8 3 4 N
Which of the following compounds is least acidic? a. I b. II c. III d. IV e. V HBr HCI NH3 ?? IV
the answers i circled are incorrect except for number 10. i know number 8 is d. for those two can you explain why the answer is that? can you give me the correct answers and explain why? ren with Down Syndrome waren with local deve we described as generat ) lam towan l and e ch rochemical court of Th correct configuration? is RS). Which offi ces corresponds OH OM HOCH,HOH I WHER TNH, CH, HO CH, w AT 111...