If a benzene ring has one methyl group as a substituent, will the next substituent add to the benzene ring in the ortho, meta, or para position? Select one: a. para or meta b. para only c. meta only d. ortho only e. ortho or meta f. Ortho or para
Benzene having methyl group means the name of the structure
is Toluene (C6H5CH3)
THE - CH3 group is weakly activating group so it activates the benzene ring by releasing the electron to the benzene ring then ortho and para positions are ready to undergoes electrophilic substitution so the incoming electrophile or substitutent attached to either ortho position or para position
answer => f . Ortho or Para
If a benzene ring has one methyl group as a substituent, will the next substituent add...
If a benzene ring has one -CF3 group as a substituent, will the next substituent add to the benzene ring in the ortho, meta, or para position? Select one: a. meta b. para only c. ortho or para d. ortho only e. cannot determine
An NH2 substituent in an aromatic ring is: Select one: a. activating ortho-, meta- and para-directing b. deactivating and ortho- and para-directing c. deactivating and meta-directing d. activating and meta-directing e. activating and ortho- and para-directing
Predict the effect the substituent attached to the benzene ring below would have on electrophilic aromatic substitution reactions? CH, CH3 a) meta director, deactivator b) ortho/para director, activator c) meta director, activator d) ortho/para director, deactivator
When there is an electron-withdrawing group on a benzene ring (eg. compounds such as nitrobenzenebenzoic acid, acetophenone, etc, resonance structures can be drawn that indicate the positions on the benzene ring that are least nucleophilic (because they have a positive charge on the carbon at that position). Because these positions are much less nucleophilic, the substitution reaction will not occur here; instead, substitution will occur at the other position(s) on the ring. As a result, which position(s) are most nucleophilic...
which of the following substituents will stabilize the charge on the carboxylic acid on the benzene ring created during hydrolysis. And why? 1. methyl group at the para postion to the carboxylic group on the benzene ring 2. methyl group at the meta position to the carboxylic acid group on the benzene ring 3. methoxy group at the meta position to the carboxylic acid group on the benene ring 4. methoxy group at the para position to the carboxylic acid...
5. Which of the following is not a meta-directing substituent when presenbt on the benzene ring? Please give explanation, too. 5. Which of the following is not a meta-directing substituent when present on the benzenering? a) -NHCOCH b) -NO2 d) -C N e).CO2H
Map. Sort the following molecules by whether the substituent group is ortho/para or meta directing for electrophilic aromatic substitution. Ortho Para Directing Meta Directing Previous Check Answer Next Exit
In a phenol, which group is the substituent on the benzene ring? a. carbonyl ]b alcohol C carboxyl d amino ts 4 ?
437 Predict whether the following substituents on the benzene ring are likely to be ha para directing or meta directing and whether they are like to be ring activating or ring deactivating deact vabang a) - NH(CH 4.38 For each of the monosabstituted benenes shown below, (1) Indicate whether the substituent is ortho, para directing or meta directing (2) Draw the structure of the main monosubstitution product for each of the reactions indicated orth. OCH3 + HCl -OCHE (fecutulys ortho...
There are 3 pictures, 18 exercises in total. Topics are Benzenes and their reactions No -I ab 0 CH3 Br nooit 1. Aromatic molecules contain Tt electrons. a. 4n b. 4n+2 c. An odd number d. 4n+1 c. Zero Condition needed for benzene halogenation to occur a. NaC1, 1120 b. C12, H20 c. C12, AICI3 d. NaCl, CH3OH e. C12, CC14 3. In an electrophilic aromatic substitution, the hydroxyl group orients ortho-para because a, removes electronic density from the benzene...