Draw a resonance structure, complete with all formal charges and lone (unshared) electron pairs, that shows the resonanceinteraction of the chloro with the para position in chlorobenzene.CIchlorobenzeneYou 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 a resonance structure, complete with all formal charges and lone (unshared) electron pairs, that shows the resonanceinteraction of the acetoxy with the para position in phenyl acetate.QeCH3phenyl 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.**O▾▼n [FPreviousNext

Cl on benzene ring is a ring deactivating group even though it is ortho para directing due to…

esona complete with interaction of the chloro with the para position in chlorobenzene. CI chlorobenzene 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. √ [F charges and lone (unshared) electron pairs, ***

esona complete with interaction of the chloro with the para position in chlorobenzene. CI chlorobenzene 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. √ [F charges and lone (unshared) electron pairs, ***

Organic Chemistry: A Guided Inquiry

2nd Edition

ISBN:9780618974122

Author:Andrei Straumanis

Publisher:Andrei Straumanis

Chapter17: Conjugation And Molecular Orbital (mo) Theory

Section: Chapter Questions

Problem 8E

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translate the bond-line notation structure to the Newman projection by filling int the missing groups (A, B, C, D or E) on the lines in the Newman projection so they match the conformation given in the original structure. Circle if the conformation is a staggered or eclipsed.
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