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5) Classify the following substituents as ELECTRON DONATING and ELECTRON WITHADRAWING? 3 PL -NH, -OCH, NO2,...
5) Classify the following substituents as ELECTRON DONATING and ELECTRON WITHADRAWING? 3R -NH, -OCH, NO, -CH3...
5) Classify the following substituents as ELECTRON DONATING and ELECTRON WITHADRAWING? 3R -NH, -OCH, NO, -CH3 Electron Donating Electron Withdrawing 6) Classify the following compounds AROMATIC, ANTI AROMATIC and NON-AROMATIC? 2 PS ☺ A) 7) Arrange the following compounds in order of decreasing reactivity towards electrophilic aromatic substitution 2 Pts so More Reactive: Least Reactive 8) Rank the following benzoic acid derivatives in the increasing order of acidity? 2P соон COOH COOH COOH OCH NO 11 III IV Weakest Acid:...
5) Classify the following substituents as ELECTRON DONATING and ELECTRON WITHADRAWING? 3R -NH, -OCH, NO, -CH3...
5) Classify the following substituents as ELECTRON DONATING and ELECTRON WITHADRAWING? 3R -NH, -OCH, NO, -CH3 Electron Donating Electron Withdrawing 6) Classify the following compounds AROMATIC, ANTI AROMATIC and NON-AROMATIC? 2 PS con A) 7) Arrange the following compounds in order of decreasing reactivity towards electrophilic aromatic substitution 2 Pts ♡ so More Reactive: Least Reactive 8) Rank the following benzoic acid derivatives in the increasing order of acidity? 2P соон COOH COOH COOH OCH NO 11 IV Weakest Acid:...
17) Write the products for the following reactions? 8 Pt A) excess сн,он. H2SO4 B) NH...
17) Write the products for the following reactions? 8 Pt A) excess сн,он. H2SO4 B) NH OH H2SO4 - C) Ph3P=CHCH3 i D) CH COOH 18) Predict the steps for the following conversion with proper reagents? (Hint: Protection and deprotection chemistry) 5 Pts осн он 5) Classify the following substituents as ELECTRON DONATING and ELECTRON WITHADRAWING? 3R -NH, -OCH, NO, -CH3 Electron Donating Electron Withdrawing 6) Classify the following compounds AROMATIC, ANTI AROMATIC and NON-AROMATIC? 2 PS con A) 7)...
1. please check what is wrong. Thank you! Determine the product formed when each compound is treated with...
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...
Can someone explain how I am supposed to know which is least reactive compared to most reactive? I know that the benzen...
Can someone explain how I am supposed to know which is least
reactive compared to most reactive? I know that the benzene with
the NO2 group on it is least reactive because it's an EWG (electron
withdrawing group) so a deactivator but how do I compare the
others? Thanks!!!
Rank the following compounds in order of their reactivity toward electrophilic aromatic substitution NO2 CH least reactive (slowest) most reactive (fastest) b
Rank the following compounds in order of their reactivity...
3.Help, this got me really confused. ORGANIC CHEMISTRY 353 UPPER LEVEL. THANKS 1. (4 pts) Arrange...
3.Help, this got me really confused. ORGANIC CHEMISTRY 353 UPPER
LEVEL. THANKS
1. (4 pts) Arrange the following compounds in order of increasing acidity (4 = most acidic): HH Meo OME 2. (4 pts.) Arrange the following in order of increasing electrophilic aromatic substitution reactivity (4 = most reactive): Br OMe 3. (4 pts.) Briefly describe why alkenes undergo addition and aromatic compounds undergo substitution. 4. (5 pts. Provide an example of an EAS reaction creates an arene that is...
True or false: a) The electron-withdrawing substituents do not impact the acidity of carboxylic acids. b)...
True or false: a) The electron-withdrawing substituents do not impact the acidity of carboxylic acids. b) Hydrolysis of nitriles is a method to synthesize carboxylic acid. c) The order of reactivity of carboxylic acid derivatives is as follow: Acyl chloride > Acid anhydride > Ester > Amide. d) SOCl2, PCl3 and PCl5 are three types of special reagents to convert carboxylic acid to acyl chloride. e) Acyl chlorides are the most reactive common acyl derivatives, and can be used to...
4.help, this got me really confused. ORGANIC CHEMISTRY 353 UPPER LEVEL. THANKS 1. (4 pts) Arrange...
4.help, this got me really confused. ORGANIC CHEMISTRY 353 UPPER
LEVEL. THANKS
1. (4 pts) Arrange the following compounds in order of increasing acidity (4 = most acidic): HH Meo OME 2. (4 pts.) Arrange the following in order of increasing electrophilic aromatic substitution reactivity (4 = most reactive): Br OMe 3. (4 pts.) Briefly describe why alkenes undergo addition and aromatic compounds undergo substitution. 4. (5 pts. Provide an example of an EAS reaction creates an arene that is...
please help in all sections asap!! In a Clemmensen reduction, an aryl ketone is reduced to...
please help in all sections asap!!
In a Clemmensen reduction, an aryl ketone is reduced to an Oaryl aldehyde Caryl alkane aryl carboxylic acid aryl ester aryi anhydride Identify the electrophile for the Friedel-Crafts acylation of benzene. O aluminum tetrachloride anion aluminum chloride acylium ion carbocation carbanion Which of the following criteria is necessary for a nucleophilic aromatic substitution reaction? © A. The ring must contain a very strong electron withdrawing group. B. The ring must contain a leaving group....
1. For the following compounds, label each substituent as electron donating or electron withdrawing, and indicate...
1. For the following compounds, label each substituent as electron donating or electron withdrawing, and indicate whether this effect is achieved via induction or resonance. ŅO2 H2N SO3H 2. Predict the TH NMR of the above benzene derivatives. For chemical shift, indicate whether the peak would likely be downfield or upfield of benzene (7.2 ppm). (Hint: think about the resonance structures that can be drawn based on your responses from above) A B # of peaks chemical shift indicate: >7.2,...
5) Classify the following substituents as ELECTRON DONATING and ELECTRON WITHADRAWING? 3R -NH, -OCH, NO, -CH3 Electron Donating Electron Withdrawing 6) Classify the following compounds AROMATIC, ANTI AROMATIC and NON-AROMATIC? 2 PS ☺ A) 7) Arrange the following compounds in order of decreasing reactivity towards electrophilic aromatic substitution 2 Pts so More Reactive: Least Reactive 8) Rank the following benzoic acid derivatives in the increasing order of acidity? 2P соон COOH COOH COOH OCH NO 11 III IV Weakest Acid:...
5) Classify the following substituents as ELECTRON DONATING and ELECTRON WITHADRAWING? 3R -NH, -OCH, NO, -CH3 Electron Donating Electron Withdrawing 6) Classify the following compounds AROMATIC, ANTI AROMATIC and NON-AROMATIC? 2 PS con A) 7) Arrange the following compounds in order of decreasing reactivity towards electrophilic aromatic substitution 2 Pts ♡ so More Reactive: Least Reactive 8) Rank the following benzoic acid derivatives in the increasing order of acidity? 2P соон COOH COOH COOH OCH NO 11 IV Weakest Acid:...
17) Write the products for the following reactions? 8 Pt A) excess сн,он. H2SO4 B) NH OH H2SO4 - C) Ph3P=CHCH3 i D) CH COOH 18) Predict the steps for the following conversion with proper reagents? (Hint: Protection and deprotection chemistry) 5 Pts осн он 5) Classify the following substituents as ELECTRON DONATING and ELECTRON WITHADRAWING? 3R -NH, -OCH, NO, -CH3 Electron Donating Electron Withdrawing 6) Classify the following compounds AROMATIC, ANTI AROMATIC and NON-AROMATIC? 2 PS con A) 7)...
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...
Can someone explain how I am supposed to know which is least
reactive compared to most reactive? I know that the benzene with
the NO2 group on it is least reactive because it's an EWG (electron
withdrawing group) so a deactivator but how do I compare the
others? Thanks!!!
Rank the following compounds in order of their reactivity toward electrophilic aromatic substitution NO2 CH least reactive (slowest) most reactive (fastest) b
Rank the following compounds in order of their reactivity...
3.Help, this got me really confused. ORGANIC CHEMISTRY 353 UPPER
LEVEL. THANKS
1. (4 pts) Arrange the following compounds in order of increasing acidity (4 = most acidic): HH Meo OME 2. (4 pts.) Arrange the following in order of increasing electrophilic aromatic substitution reactivity (4 = most reactive): Br OMe 3. (4 pts.) Briefly describe why alkenes undergo addition and aromatic compounds undergo substitution. 4. (5 pts. Provide an example of an EAS reaction creates an arene that is...
4.help, this got me really confused. ORGANIC CHEMISTRY 353 UPPER
LEVEL. THANKS
1. (4 pts) Arrange the following compounds in order of increasing acidity (4 = most acidic): HH Meo OME 2. (4 pts.) Arrange the following in order of increasing electrophilic aromatic substitution reactivity (4 = most reactive): Br OMe 3. (4 pts.) Briefly describe why alkenes undergo addition and aromatic compounds undergo substitution. 4. (5 pts. Provide an example of an EAS reaction creates an arene that is...
please help in all sections asap!!
In a Clemmensen reduction, an aryl ketone is reduced to an Oaryl aldehyde Caryl alkane aryl carboxylic acid aryl ester aryi anhydride Identify the electrophile for the Friedel-Crafts acylation of benzene. O aluminum tetrachloride anion aluminum chloride acylium ion carbocation carbanion Which of the following criteria is necessary for a nucleophilic aromatic substitution reaction? © A. The ring must contain a very strong electron withdrawing group. B. The ring must contain a leaving group....
1. For the following compounds, label each substituent as electron donating or electron withdrawing, and indicate whether this effect is achieved via induction or resonance. ŅO2 H2N SO3H 2. Predict the TH NMR of the above benzene derivatives. For chemical shift, indicate whether the peak would likely be downfield or upfield of benzene (7.2 ppm). (Hint: think about the resonance structures that can be drawn based on your responses from above) A B # of peaks chemical shift indicate: >7.2,...
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