Select the keyword or phrase that will best complete each sentence. Key terms: backside carbocation elimination frontside hyperconjugation inversion maintenance nucleophile product racemization stronger substitution weaker Alkyl halides undergo A orbital. reactions with Brønsted-Lowry bases. is a sp² hybridized and trigonal planar and contains a vacant p All SN2 reactions proceed with in attack of the nucleophile, resulting of configuration at a stereognic center. Spreading out charge by the overlap of an empty p orbital with an adjacent o bond is called Equilibrium favors the products of nucleophilic substitution when the leaving group is a base than the nucleophile. According the to Hammond postulate, the stability of the determines the rate of its formation. The formation of equal amounts of two enantiomeric products from a single starting material is called A is an electron-rich compound, which donates a pair of electrons to an electron deficient compound, forming a covalent bond. www
Select the keyword or phrase that will best complete each sentence. Key terms: backside carbocation elimination frontside hyperconjugation inversion maintenance nucleophile product racemization stronger substitution weaker Alkyl halides undergo A orbital. reactions with Brønsted-Lowry bases. is a sp² hybridized and trigonal planar and contains a vacant p All SN2 reactions proceed with in attack of the nucleophile, resulting of configuration at a stereognic center. Spreading out charge by the overlap of an empty p orbital with an adjacent o bond is called Equilibrium favors the products of nucleophilic substitution when the leaving group is a base than the nucleophile. According the to Hammond postulate, the stability of the determines the rate of its formation. The formation of equal amounts of two enantiomeric products from a single starting material is called A is an electron-rich compound, which donates a pair of electrons to an electron deficient compound, forming a covalent bond. www
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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Transcribed Image Text:Select the keyword or phrase that will best complete each sentence.
Key terms:
backside
carbocation
elimination
frontside
hyperconjugation
inversion
maintenance
nucleophile
product
racemization
stronger
substitution
weaker
Alkyl halides undergo
A
orbital.
reactions with Brønsted-Lowry bases.
is a sp² hybridized and trigonal planar and contains a vacant p
All SN2 reactions proceed with
in
attack of the nucleophile, resulting
of configuration at a stereognic center.
Spreading out charge by the overlap of an empty p orbital with an adjacent o bond
is called
Equilibrium favors the products of nucleophilic substitution when the leaving group
is a
base than the nucleophile.
According the to Hammond postulate, the stability of the
determines the rate of its formation.
The formation of equal amounts of two enantiomeric products from a single starting
material is called
A
is an electron-rich compound, which donates a pair of electrons
to an electron deficient compound, forming a covalent bond.
‒‒‒
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