List of the following compound according to their reactivity towards electrophilic substitution.
Generally Benzene and it's it's derivatives undergo Electrophilic substitution reactions. It needs more electron density on benzene ring. Donating groups increases the electron density hence more reactive.
Withdrawing group decreases the reactivity.
A. O-dibromo benzene> bromobenzene> benzene
B. P-methoxy benzonitrile> p-methylbenzonittrile> benzonitrile
C. O-xylene> fluorobenzene> Benzaldehyde
NO2 is a strong withdrawing group and decresdec the electron density on benzene ring hence further Electrophilic substitution doesn't occurs.
List of the following compound according to their reactivity towards electrophilic substitution. 072) List the following...
4) Rank the compounds in each group according to their reactivity toward electrophilic aromatic substitution a) Benzene, benzenesulfonic acid, o-dibromobenzene a) p-Bromotoluene, nitrobenzene, aniline a) o-Xylene, phenol, benzaldehyde
Question 2 0.5 pts Rank each group of aromatic compounds according to their reactivity toward electrophilic substitution: a. Benzonitrile, p-methylbenzonitrile, p-methoxybenzonitrile b. Fluorobenzene, benzaldehyde, o-xylene c. Phenol, nitrobenzene, p-cyanonitrobenzene
!!! If each compound undergoes electrophilic aromatic substitution, where should the substituent be added? *The choices for each are either ortho/para position OR meta position.* Phenol? Benzaldehyde? Benzoic Acid? Bromobenzene? Nitrobenzene? Toluene?
Consider the reactivity of phenol, bromobenzene, toluene, and nitrobenzene toward electrophilic aromatic substitution. 1.) The most reactive compound is (pick one: phenol, bromobenzene, toluene, and nitrobenzene) because the (pick one: electron donating or electron withdrawing) character of the (pick one: alcohol group, methyl group, bromine atom, or nitro group) increases the rate of the reaction. 2.) The least reactive compound is (pick one: phenol, bromobenzene, toluene, and nitrobenzene) because the (pick one: electron donating or electron withdrawing) character of the...
organic chemistry
Question 8 Which of the following compound is more reactive than benzene in electrophilic aromatic substitution? O A methylbenzene ОВ. bromobenzene oc benzaldehyde OD. chlorobenzene O E nitrobenzene
In the following compound, select the position that is most
reactive towards electrophilic aromatic substitution
reaction.
Review of Skills - Skill Builder 18.03 X Incorrect. Tert-butyl (activator) will direct the incoming electrophile and it is an ortho-para director. In the following compound, select the position that is most reactive towards electrophilic aromatic substitution reaction. NO,
1. please check what is wrong. Thank you!
Determine the product formed when each compound is treated with Br2 and FeBr3. Drag the atom labels to their appropriate positions. CN Atom labels H H Br Br2 A. FeBr Br H OH OH Br Br. Br2 FeBr3 H H Br Br H Br2 FeBr H1 H Reset T Rank the compounds in each group in order of decreasing reactivity in electrophilic aromatic substitution. CI Decreasing reactivity Rank the compounds in each...
250 ChemActivity 29 Electrophilic Aromatic Substitution no ChemActivity 29 Part A: Electrophilic Aromatic Substitution (What products are formed when a strong electrophile is added to benzene?) Model 1: (review) Electrophilic Addition of HCI Rani o g cyclohexene carbocation intermediate Run 2 U X benzene This product carbocation intermediate DOES NOT Critical Thinking Questions 1 For Rxn I (above) draw curved arrows showing the mechanism of electrophilic addition of HCl. Include an appropriate carbocation intermediate in the box above. Figure 1:...
organic chemistry 353
2. (4 pts.) Arrange the following in order of increasing electrophilic aromatic substitution reactivity (4 = most reactive): SO3H OH e 3. (4 pts.) Briefly describe why alkenes undergo addition and aromatic compounds undergo substitution. n Briefly describe w 4. (5 pts. Provide an example of an EAS reaction creates an arene that is less reactive than benzene (be specific, include reagents, you do not need to show the mechanism)
PLEASE ANSWER ALL QUESTIONS
34) Which sequence correctly ranks the following aromatic rings in order of increasing rate of reactivity in an electrophilic aromatic substitution reaction? LOCH A) 1<2<3 B) 2 <3 <1 C) 3 <1<2 D) 2 <1<3 35) Derivatives of the compound shown below are currently being examined for their effectiveness in treating drug addiction and metabolic syndrome (J. Med. Chem. 2006, 872). Which sequence ranks the following aromatic rings of this compound in order of increasing reactivity...