[Review Topics] [References) 1. H,SO, / H2O H20 Mg Br HSO, 2. HO. Na HCO, Na CO2 H2O h SN1 Nucleophilic substitution i = SN2 Nucleophilic substitution-. j Electrophilic aromatic substitution a = Proton transfer e = Electrophilic addition f El Elimination b Lewis acid/base c = Radical chain substitution d Radical chain addition g = E2 Elimination Identify the mechanism by which each of the reactions above proceeds from among the mechanisms listed. Use the letters a - j for your answers. 1. 2. Submit Answer Retry Entire Group 9 more group attempts remaining Previous Next Email Instructor Save and Exi
Electronic Effects
The effect of electrons that are located in the chemical bonds within the atoms of the molecule is termed an electronic effect. The electronic effect is also explained as the effect through which the reactivity of the compound in one portion is controlled by the electron repulsion or attraction producing in another portion of the molecule.
Drawing Resonance Forms
In organic chemistry, resonance may be a mental exercise that illustrates the delocalization of electrons inside molecules within the valence bond theory of octet bonding. It entails creating several Lewis structures that, when combined, reflect the molecule's entire electronic structure. One Lewis diagram cannot explain the bonding (lone pair, double bond, octet) elaborately. A hybrid describes a combination of possible resonance structures that represents the entire delocalization of electrons within the molecule.
Using Molecular Structure To Predict Equilibrium
Equilibrium does not always imply an equal presence of reactants and products. This signifies that the reaction reaches a point when reactant and product quantities remain constant as the rate of forward and backward reaction is the same. Molecular structures of various compounds can help in predicting equilibrium.
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[Review Topics]
[References]
1.
Br
H,SO, /H,O
H20
Mg2+
Br
HSO,
2.
OH
Na HCO,
O Na
CO2
H20
h = Sy1 Nucleophilic substitution
i= SN2 Nucleophilic substitution-
j= Electrophilic aromatic substitution
a = Proton transfer
e = Electrophilic addition
b = Lewis acid/base
f= El Elimination
c = Radical chain substitution
d = Radical chain addition
g = E2 Elimination
Identify the mechanism by which each of the reactions above proceeds from among the mechanisms listed.
Use the letters a - j for your answers.
2.
Submit Answer
Retry Entire Group
9 more group attempts remaining
Previous
Next
Email Instructor
Save and Exi
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