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ch 22
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Draw the most stable resonance form for the intermediate...
ch 22 Draw the most stable resonance form for the intermediate in the following electrophilic substitution...
ch 22
Draw the most stable resonance form for the intermediate in the following electrophilic substitution reaction. In progress OCH OCH3 CH3CI / AICI: HC • You do not have to consider stereochemistry • Include all valence lone pairs in your answer . In cases where there is more than one answer, just draw one С P he (1 (Review Topics (References Draw the most stable resonance form for the intermediate in the following electrophilic substitution reaction. CHE -CH₂ CH,CI...
Draw the most stable resonance form for the intermediate in the following electrophilic substitution reaction. CH3COCI...
Draw the most stable resonance form for the intermediate in the following electrophilic substitution reaction. CH3COCI / AICI: CH3 CH30 CH30 • You do not have to consider stereochemistry. Include all valence lone pairs in your answer. • In cases where there is more than one answer, just draw one. . Draw the most stable resonance form for the intermediate in the following electrophilic substitution reaction. CI CI HNO3 / H2SO4 ON • You do not have to consider stereochemistry....
Draw the least stable resonance form for the intermediate in the following electrophilic substitution reaction. NO2...
Draw the least stable resonance form for the intermediate in the following electrophilic substitution reaction. NO2 NO2 Brz/ FeBrz Br . You do not have to consider stereochemistry. Include all valence lone pairs in your answer. • In cases where there is more than one answer, just draw one. . с ору P aste [] Previous NE Draw the most stable resonance form for the intermediate in the following electrophilic substitution reaction. OH OH CH3 CH3 CH2 H3PO4 CH3 H3C...
Draw the least stable resonance form for the intermediate in the following electrophilic substitution reaction. Brz/...
Draw the least stable resonance form for the intermediate in the following electrophilic substitution reaction. Brz/ FeBrz CH3 Br • You do not have to consider stereochemistry. • Include all valence lone pairs in your answer. • In cases where there is more than one answer, just draw one.
ch 22 says my ans is wrong (Review TODICE [References Draw a resonance structure, complete with...
ch 22
says my ans is wrong
(Review TODICE [References Draw a resonance structure, complete with all formal charges and lone (unshared) electron pairs, that shows the resonance interaction of the acetoxy with the para position in phenyl acetate. ubmitted aula CH3 phenyl acetate • You do not have to consider stereochemistry . Include all valence lone pairs in your answer. • In cases where there is more than one answer, just draw one. P opy С Draw a resonande...
ch 22 Draw a resonance structure, complete with all formal charges and lone (unshared) electron pairs,...
ch 22
Draw a resonance structure, complete with all formal charges and lone (unshared) electron pairs, that shows the resonance interaction of the carboxy with the para position in benzoic acid. OH benzoic acid • You do not have to consider stereochemistry. • Include all valence lone pairs in your answer. • In cases where there is more than one answer, just draw one. с P opy to // [Review Topics IReferences Draw a resonance structure, complete with all formal...
References [Review Topical Acyl transfer (nucleophilic substitution at carbonyl) reactions proceed in two stages via a...
References [Review Topical Acyl transfer (nucleophilic substitution at carbonyl) reactions proceed in two stages via a "tetrahedral intermediate." Draw the tetrahedral intermediate as it is first formed in the following reaction CH3OH H2SO4 (trace) reflux • You do not have to consider stereochemistry • Include all valence lone pairs in your answer. • Do not include counter-ions, e.g, Na, I. in your answer. • In cases where there is more than one answer, just draw one. - -O0O- (Review Topical...
Draw a second resonance from for the structure shown below. Draw a second resonance form for...
Draw a second resonance from for the structure shown below.
Draw a second resonance form for the structure shown below. CH3 I • Include all valence lone pairs in your answer. • In cases where there is more than one answer, just draw one. • Should you want to restart the exercise, the drop-down menu labeled == starting points == can be used to redraw the starting molecule on the sketcher. • In your structure, all second row elements should...
circle ans please NaOH, HO N(CH3)2 a. Draw the structure of the tetrahedral intermediate INITIALLY-FORMED in...
circle ans please
NaOH, HO N(CH3)2 a. Draw the structure of the tetrahedral intermediate INITIALLY-FORMED in the reaction shown. . You do not have to consider stereochemistry • Do not include counter-ions, e.g. Nat. 1, in your answer. • In cases where there is more than one answer, just draw one. opy ste C 000 ( b. Draw the structures of the organic products of the acyl transfer reaction. • You do not have to consider stereochemistry • Draw the...
During electrophilic aromatic substitution, a resonance-stabilized cation intermediate is formed. Groups, already present on the benzene...
During electrophilic aromatic substitution, a resonance-stabilized cation intermediate is formed. Groups, already present on the benzene ring, that direct ortho/para further stabilize this intermediate by participating in the resonance delocalization of the positive charge. Assume that the following group is present on a benzene ring at position 1 and that you are brominating the ring at positon 4. In the box below draw the structure of the resonance contributor that shows this group actively participating in the charge delocalization. -OCH3...
ch 22
Draw the most stable resonance form for the intermediate in the following electrophilic substitution reaction. In progress OCH OCH3 CH3CI / AICI: HC • You do not have to consider stereochemistry • Include all valence lone pairs in your answer . In cases where there is more than one answer, just draw one С P he (1 (Review Topics (References Draw the most stable resonance form for the intermediate in the following electrophilic substitution reaction. CHE -CH₂ CH,CI...
Draw the most stable resonance form for the intermediate in the following electrophilic substitution reaction. CH3COCI / AICI: CH3 CH30 CH30 • You do not have to consider stereochemistry. Include all valence lone pairs in your answer. • In cases where there is more than one answer, just draw one. . Draw the most stable resonance form for the intermediate in the following electrophilic substitution reaction. CI CI HNO3 / H2SO4 ON • You do not have to consider stereochemistry....
Draw the least stable resonance form for the intermediate in the following electrophilic substitution reaction. NO2 NO2 Brz/ FeBrz Br . You do not have to consider stereochemistry. Include all valence lone pairs in your answer. • In cases where there is more than one answer, just draw one. . с ору P aste [] Previous NE Draw the most stable resonance form for the intermediate in the following electrophilic substitution reaction. OH OH CH3 CH3 CH2 H3PO4 CH3 H3C...
Draw the least stable resonance form for the intermediate in the following electrophilic substitution reaction. Brz/ FeBrz CH3 Br • You do not have to consider stereochemistry. • Include all valence lone pairs in your answer. • In cases where there is more than one answer, just draw one.
ch 22
says my ans is wrong
(Review TODICE [References Draw a resonance structure, complete with all formal charges and lone (unshared) electron pairs, that shows the resonance interaction of the acetoxy with the para position in phenyl acetate. ubmitted aula CH3 phenyl acetate • You do not have to consider stereochemistry . Include all valence lone pairs in your answer. • In cases where there is more than one answer, just draw one. P opy С Draw a resonande...
ch 22
Draw a resonance structure, complete with all formal charges and lone (unshared) electron pairs, that shows the resonance interaction of the carboxy with the para position in benzoic acid. OH benzoic acid • You do not have to consider stereochemistry. • Include all valence lone pairs in your answer. • In cases where there is more than one answer, just draw one. с P opy to // [Review Topics IReferences Draw a resonance structure, complete with all formal...
References [Review Topical Acyl transfer (nucleophilic substitution at carbonyl) reactions proceed in two stages via a "tetrahedral intermediate." Draw the tetrahedral intermediate as it is first formed in the following reaction CH3OH H2SO4 (trace) reflux • You do not have to consider stereochemistry • Include all valence lone pairs in your answer. • Do not include counter-ions, e.g, Na, I. in your answer. • In cases where there is more than one answer, just draw one. - -O0O- (Review Topical...
Draw a second resonance from for the structure shown below.
Draw a second resonance form for the structure shown below. CH3 I • Include all valence lone pairs in your answer. • In cases where there is more than one answer, just draw one. • Should you want to restart the exercise, the drop-down menu labeled == starting points == can be used to redraw the starting molecule on the sketcher. • In your structure, all second row elements should...
circle ans please
NaOH, HO N(CH3)2 a. Draw the structure of the tetrahedral intermediate INITIALLY-FORMED in the reaction shown. . You do not have to consider stereochemistry • Do not include counter-ions, e.g. Nat. 1, in your answer. • In cases where there is more than one answer, just draw one. opy ste C 000 ( b. Draw the structures of the organic products of the acyl transfer reaction. • You do not have to consider stereochemistry • Draw the...
During electrophilic aromatic substitution, a resonance-stabilized cation intermediate is formed. Groups, already present on the benzene ring, that direct ortho/para further stabilize this intermediate by participating in the resonance delocalization of the positive charge. Assume that the following group is present on a benzene ring at position 1 and that you are brominating the ring at positon 4. In the box below draw the structure of the resonance contributor that shows this group actively participating in the charge delocalization. -OCH3...
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