Chapter 8: 8-2 TP (page 383)
Draw the resonance contributors for the following carbocation
Chapter 8: 8-2 TP (page 383)
Draw the resonance contributors for the following carbocation
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Get started for freeThe acid dissociation constant (Ka) for loss of a proton from cyclohexanol is 1 ×10-16.
a. Draw a reaction coordinate diagram for loss of a proton from cyclohexanol.
b. Draw the resonance contributors for phenol.
c. Draw the resonance contributors for the phenolate ion.
d. On the same plot with the energy diagram for loss of a proton from cyclohexanol, draw an energy diagram for loss of a proton from phenol.
e. Which has a greater Ka: cyclohexanol or phenol?
f. Which is a stronger acid: cyclohexanol or phenol?
Rank the indicated hydrogen in the following compounds from most acidic to least acidic:
Identify the kinetic and thermodynamic products of the following reaction:
a. Draw resonance contributors for the following species, showing all the lone pairs:
1.CH2N2 2. N2O 3. NO2-
b. For each species, indicate the most stable resonance contributor.
a. Which oxygen atom has the greater electron density?
b. Which compound has the greater electron density on its nitrogen atom?
c. Which compound has the greater electron density on its oxygen atom?
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