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Electron Withdrawing Groups Solutions Library

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40 solutions

Electron Withdrawing Groups

Q. Draw structural formulas for the major organic product(s) of the reaction shown below.

Solved • Oct 25, 2018

Electron Withdrawing Groups

Q. What is (are) the product(s)?

Solved • Jun 25, 2018

Electron Withdrawing Groups

Q. For the following reaction, draw the major organic product(s). Do not draw inorganic side products.

Solved • Jun 18, 2018

Electron Withdrawing Groups

Q. Draw the major product(s) that result from the following reaction. Do not draw inorganic side products.

Solved • Jun 8, 2018

Electron Withdrawing Groups

Q. Give the structures of the two major products in the following reaction.

Solved • Jun 8, 2018

Electron Withdrawing Groups

Q. Draw the major organic product(s) for the following reaction. Multiple products may be drawn in one box, in any order. Use an expanded octet around...

Solved • Jun 8, 2018

Electron Withdrawing Groups

Q. Draw the structure of the product in the following reaction of aniline with CH3CI in the presence of AICI3. Be sure to show formal charges, if appl...

Solved • Jun 8, 2018

Electron Withdrawing Groups

Q. Draw the major organic product(s) for the following reaction. Multiple products may be drawn in one box, in any order. Include charges as needed.

Solved • Jun 5, 2018

Electron Withdrawing Groups

Q. Draw the major organic product(s) for the following Friedel-Crafts acylation reaction: 

Solved • May 29, 2018

Electron Withdrawing Groups

Q. Draw the structure of the expected major organic product if this compound was to undergo monobromination with Br2/FeBr3. You do not have to conside...

Solved • May 17, 2018

Electron Withdrawing Groups

Q. Draw the major product(s) that result from the following reaction. Do not draw inorganic side products.

Solved • May 12, 2018

Electron Withdrawing Groups

Q. The following compounds are treated with HNO3/H2SO4. Predict the positions of electrophilic attack that lead to the major nitration product(s). 

Solved • May 11, 2018

Electron Withdrawing Groups

Q. Predict the major product for the following reaction.

Solved • May 8, 2018

Electron Withdrawing Groups

Q. Draw the major organic product(s) for the following reaction. Multiple products may be drawn in one box, in any order. Use an expanded octet around...

Solved • May 4, 2018

Electron Withdrawing Groups

Q. Which one of the following would most readily undergo electrophilic aromatic substitution with an electrophile E+?

Solved • Dec 21, 2017

Electron Withdrawing Groups

Q. Provide the expected major product (One-Step EAS):

Solved • Dec 21, 2017

Electron Withdrawing Groups

Q. Provide the expected major product (One-Step EAS):

Solved • Dec 21, 2017

Electron Withdrawing Groups

Q. Provide the expected major product (One-Step EAS):

Solved • Dec 21, 2017

Electron Withdrawing Groups

Q. Supply the mechanism and structure of the major product of the following EAS reaction.

Solved • Dec 20, 2017

Electron Withdrawing Groups

Q. Which of the following compounds is most deactivated toward elimination-addition Electrophilic Aromatic Substituted with an electrophile E+?

Solved • Dec 20, 2017

Electron Withdrawing Groups

Q. The major product of the following reaction is 

Solved • Jun 20, 2017

Electron Withdrawing Groups

Q. Methyl p-nitrobenzoate has been found to undergo saponification (hydrolysis) faster than methyl benzoate. a. Consider the mechanism of saponificati...

Solved • Jun 6, 2017

Electron Withdrawing Groups

Q. Complete the following reaction by drawing the structure of the principal major product. Indicate relative stereochemistry where necessary. If ther...

Solved • May 26, 2017

Electron Withdrawing Groups

Q. Complete the following reaction by drawing the structure of the principal major product. Indicate relative stereochemistry where necessary. If ther...

Solved • May 26, 2017

Electron Withdrawing Groups

Q. It's dipole roundup! Indicate which of the molecules have EDGs with an asterisk, EWGs with a check mark, o,p-directors with a circle, and meta-dire...

Solved • May 8, 2017

Electron Withdrawing Groups

Q. Which one of the following compounds will be least reactive towards Friedel-Crafts reaction? a. nitrobenzene b. anisole c. phenol d. benzene e...

Solved • Dec 21, 2016

Electron Withdrawing Groups

Q. In electrophilic aromatic substitution reactions the hydroxyl group is an o,p-director because: a. it donates electron density to the ring by indu...

Solved • Dec 21, 2016

Electron Withdrawing Groups

Q. Which of the following compounds reacts most slowly during nitration?

Solved • Dec 21, 2016

Electron Withdrawing Groups

Q. In electrophilic aromatic substitution reactions a bromine substituent: a. a is a deactivator and a m-director b. b is a deactivator and an o,p-d...

Solved • Dec 21, 2016

Electron Withdrawing Groups

Q. Which of the following is the major product of the reaction below?

Solved • Nov 2, 2016

Electron Withdrawing Groups

Q. Which one of the following compounds would be most reactive toward electrophilic aromatic substitution?

Solved • Nov 2, 2016

Electron Withdrawing Groups

Q. Circle the compound that would react the fastest in a typical electrophilic aromatic substitution reaction (most activated aromatic ring)   

Solved • Aug 4, 2016

Electron Withdrawing Groups

Q. Which statement best describes why anisole brominates faster than benzene?A) The inductive effect of the methoxy group stabilizes the cationic inte...

Solved • May 8, 2016

Electron Withdrawing Groups

Q. Which substituents would deactivate benzene toward electrophilic aromatic substitution reactions?

Solved • May 8, 2016

Electron Withdrawing Groups

Q. Rank 1, 2, 3 and 4 (1 = fastest to 4 = slowest) the following compounds in order of reactivity toward electrophilic aromatic substitution by writin...

Solved • Apr 21, 2016

Electron Withdrawing Groups

Q. Which reagent would you use to carry out the following transformation?tert-butylbenzene → p-tert-butylbenzenesulfonic acid   +   o-tert-butylbenzen...

Solved • Apr 4, 2016

Electron Withdrawing Groups

Q. Circle the benzene rings with a deactivating group. Star (*) the benzene rings with an ortho/para‐directing group. 

Solved • Mar 14, 2016

Electron Withdrawing Groups

Q. Which compound has the slowest rate toward an electrophilic aromatic substitution reaction?a) chlorobenzeneb) toluenec) benzened) nitrobenzenee) an...

Solved • Feb 19, 2016

Electron Withdrawing Groups

Q. Predict the major product for each of the following reactions paying attention to the region- and stereochemistry. If there is no reaction, write j...

Solved • Feb 1, 2016

Electron Withdrawing Groups

Q. Which compound is more reactive than benzene in electrophilic aromatic substitution reaction?   a. benzaldehyde b. nitrobenzene c. toluene d. ...

Solved • Feb 1, 2016