An allylic substrate is more favorable for unimolecular E1/Sn1 reactions than a 3° substrate because relative to the 3° carbocation the allylic carbocation is in energy because it's by resonance. O A. lower; destabilized OB. lower; stabilized OC. higher; destabilized O D. higher; stabilized

An allylic substrate is more favorable for unimolecular E1/Sn1 reactions than a 3° substrate because relative to the 3° carbocation the allylic carbocation is in energy because it's by resonance. O A. lower; destabilized OB. lower; stabilized OC. higher; destabilized O D. higher; stabilized

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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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.

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An allylic substrate is more favorable for unimolecular E1/Sn1 reactions than a 3° substrate because relative to the 3° carbocation the allylic carbocation is ----------- in energy
because it's ---------- by resonance.
O A. lower; destabilized
OB. lower; stabilized
OC. higher; destabilized
O D. higher; stabilized

If 2-iodobutane had been used to alkylate saccharin instead of iodoethane the reaction would have been
O A. slower; an achiral product
OB. faster; a racemic mixture
OC. slower; a racemic mixture
O D. faster; an achiral product
and would have produced

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