17. a. Label the reactive features, highlight the most reactive one, then highlight what it needs.Also, state if the reaction will start to create a carbocation, carbon radical, or carbanion, or willcause loss of aromatic character. If a carbocation, carbon radical, or carbanion starts todevelop, label where that will occur.CH3with Cl, and FeCl,CH2 CH3b. Use mechanism arrows to illustrate the reaction that occurs.c. If applicable, use stabilization resources to deal with the carbocation, carbon radical, orcarbanion that starts to develop during the reaction, and draw the structure of anyresonance-stabilized intermediate.d. Continue labeling and diagramming the reaction until you find the major stable product(s).e. Finally, state the stereochemistry of the major product(s) and use either Fisher projectionor perspective formula representations to illustrate that stereochemistry.

Solution : Electrophilic aromatic substitution reaction involves 3 steps as given below :…

17. a. Label the reactive features, highlight the most reactive one, then highlight what it needs. Also, state if the reaction will start to create a carbocation, carbon radical, or carbanion, or will cause loss of aromatic character. If a carbocation, carbon radical, or carbanion starts to develop, label where that will occur. -CH3 with Cl, and FeCl, CH2 CH3

17. a. Label the reactive features, highlight the most reactive one, then highlight what it needs. Also, state if the reaction will start to create a carbocation, carbon radical, or carbanion, or will cause loss of aromatic character. If a carbocation, carbon radical, or carbanion starts to develop, label where that will occur. -CH3 with Cl, and FeCl, CH2 CH3

Chemistry

10th Edition

ISBN:9781305957404

Author:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste

Publisher:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste

Chapter1: Chemical Foundations

Section: Chapter Questions

Problem 1RQ: Define and explain the differences between the following terms. a. law and theory b. theory and...

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Concept explainers

Alkanes and Cycloalkanes

Alkanes are saturated organic compounds which are made up of C and H atoms. Alkanes have the general formula of CnH2n+2. Alkane contains sp3 hybridized carbon atoms with four sigmas (σ) bonds & every hydrogen atom is connected with one of the carbon atoms. The size of the alkane could be determined by the number of carbon atoms located in it.

Question

17. a. Label the reactive features, highlight the most reactive one, then highlight what it needs.
Also, state if the reaction will start to create a carbocation, carbon radical, or carbanion, or will
cause loss of aromatic character. If a carbocation, carbon radical, or carbanion starts to
develop, label where that will occur.
CH3
with Cl, and FeCl,
CH2 CH3
b. Use mechanism arrows to illustrate the reaction that occurs.
c. If applicable, use stabilization resources to deal with the carbocation, carbon radical, or
carbanion that starts to develop during the reaction, and draw the structure of any
resonance-stabilized intermediate.
d. Continue labeling and diagramming the reaction until you find the major stable product(s).
e. Finally, state the stereochemistry of the major product(s) and use either Fisher projection
or perspective formula representations to illustrate that stereochemistry.

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