Name: TA: Partner: 1) Arrange the assigned benzene substituents in order of reactivity in EAS reactions....

Question

Question

Name: TA: Partner: 1) Arrange the assigned benzene substituents in order of reactivity in EAS reactions. Explain the trend (1

science chemistry

Add a comment Improve this question Transcribed image text

Answer 1

Answer #1

E +M .. . NA С - Сн NH (CH₂ CH₂ +ILoup -I 100 (в мг 1 group co-CH₂ Order of reactivity [b>a>c>d]

+M group activate the ring for EAS reaction and -M deactivate the ring for EAS.
+I increase +M and -I decrease +M.
-S weak activating group.

The order of reactivity-

b > a > c > d

Please hit the upthumb.

Add a comment

Answer 2

Similar Homework Help Questions

Name: TA: Partner: 1) Arrange the assigned benzene substituents in order of reactivity in EAS reactions....

Name: TA: Partner: 1) Arrange the assigned benzene substituents in order of reactivity in EAS reactions. Explain the trend (1.5 points) 2) Use your knowledge of resonance, aromaticity, and general stability trends to analyze the following sets of reactions, explain why each reaction is fast or slow (1.5 points) CH3OH CH3OH fast slow + Br Lab 6! Chemistry Of Aromatic Compounas Part 2: 2) Starting with a compound with 6 (or less carbons) propose a synthesis for the assigned compounds....
1) Arrange the assigned benzene substituents in order of reactivity in EAS reactions. Explain the trend...

1) Arrange the assigned benzene substituents in order of reactivity in EAS reactions. Explain the trend (1.5 points) pro mo ph Ph-M Ph-8
1) Arrange the assigned benzene substituents in order of reactivity in EAS reactions. Explain the trend...

1) Arrange the assigned benzene substituents in order of reactivity in EAS reactions. Explain the trend (1 points) 2) Use your knowledge of resonance, aromaticity, and general stability trends to analyze the following sets of reactions, explain why each reaction is fast or slow (1 points) CH3OH CH3OH fast slow 2) Starting with a compound with 6 (or less carbons) propose a synthesis for the assigned compounds. Provide all reagents and show intermediates (2 points) | 4) Provide all the...

Arrange the following in order of decreasing reactivity towards hydrolysis using aqueous NaOH and explain this...

Arrange the following in order of decreasing reactivity towards hydrolysis using aqueous NaOH and explain this trend. (1.5) (a) CH3CO2CH3 (b) CH3COCI (c) CH3CON(CH3)2 (d) CH3CO2COCH3
1. arrange the halides in order of reactivity under the two sets of conditions Part 2:...

1. arrange the halides in order of reactivity under the two sets of conditions Part 2: A Comparison of the Reactivity of Alkyl Halides 2% ethanolic silver nitrate 15 Nal in acetone 1. n-butyl chloride Clear Milky precipitate 2. sec-butyl chloride After heating, some precipitation 3. t-butyl chloride White precipitate After heating, precipitate Clear No precipitate Milk precipitate 4. n-butyl bromide Clear 5. allyl chloride White precipitate Brown color precipitate 6. chlorobenzene Clear Clear 1. Arrange the halides in order...
Predict the relative order of reactivity of the indicated carbonyl compounds in reactions with nucleophiles (1...

Predict the relative order of reactivity of the indicated carbonyl compounds in reactions with nucleophiles (1 = most reactive carbonyl electrophile). Use all three logic arguments of organic chemistry (resonance, inductive and steric). Show structures, lone pairs and arrow-pushing conventions in your answer to provide an explanation for your order of reactivity. Write the expected product in a reaction with lithium aluminium deuteride, LiAlD4, followed by workup (no mechanisms) Name 2. Predict the relative order of reactivity of the indicated...

1. Draw the line structures and arrange the following substrates in order of increasing SN2 reactivity...

1. Draw the line structures and arrange the following substrates in order of increasing SN2 reactivity with NaCN: Bromoethane, 1-chloro-3,3-dimethylpentane, 1-chloro-2,2-dimethylpentane, and 2-bromo-2- methylpentane. (1 pt) 2. Design a synthetic route for the following conversion of methylcylohexane into compound A using retrosynthesis analysis. You may use any other reagents that you need. (1 pt) 3. Predict which of the following two compounds will undergo an E2 reaction more rapidly in presence of EtONa/EtOH. Draw the reaction product(s) and the mechanism...
8. Rank these compounds in decreasing order of their reactivity in SN 1 reactions. (8 points)

8. Rank these compounds in decreasing order of their reactivity in SN 1 reactions. (8 points)
Arrange the following chloroalkanes in order of increasing reactivity towards a S_N1 reaction: 1-chloro-2-methylbutane, 1-chloro-3-methylbutane, 2-chloro-2-methylbutane,...

Arrange the following chloroalkanes in order of increasing reactivity towards a S_N1 reaction: 1-chloro-2-methylbutane, 1-chloro-3-methylbutane, 2-chloro-2-methylbutane, 1-chloropentane (A complete answer will provide a bond line drawing of each of the compounds listed) For the same compounds found in question 1, list them in order of increasing reactivity towards an S_N2 reaction (list them as structures as well) Provide a bond line drawing of the product for the following reactions: (answer on back) a. (2S)-2-bromobutane + NaCN in acetone b. (3R)-3-iodo-1...

JI) Name the compounds or draw the structures from their names. (2 pts) 1,2-chovo mul COOH...

JI) Name the compounds or draw the structures from their names. (2 pts) 1,2-chovo mul COOH a) NO2 b) CI c) 4-phenyl-2-pentanol; •DH d) 1-bromo-2-chloro-4-ethylbenzene; 2. Arrange the compounds in each set in order of decreasing reactivity (fastest to slowest) toward EAS. Explain. (2 pts) 0-C-CH3 -C-0-CH3 a) (A) (B) (C) CH2CH3 -NH2 ( C1) do nosotros (B) b) (A) 3. Account for the observation that trifluoromethyl groups is meta directing, as shown in the following example. (1 pt) CF3...

Name: TA: Partner: 1) Arrange the assigned benzene substituents in order of reactivity in EAS reactions....

Homework Answers