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Worksheetschapter 3-orgchem
Total questions: 71
Worksheet time: 37mins
bond cleavage reaction for ions
homorolytic
heterolytic
bond cleavage reaction for radicals
homorolytic
heterolytic
left side of the equation is _____ centered free radical
carbon
hydrogen
right side of the equation is ________ centered radical
carbon
hydrogen
which has the shortest life
radical
carbanion
carbene
carbocation
which has the longest life
radical
carbanion
carbene
carbocation
which has the second longest life
radical
carbanion
carbene
carbocation
which is an acid
carbanion
carbocation
radical
carbene
which is an lewis base
carbanion
carbocation
radical
carbene
which is neutral
carbanion
carbocation
radical
carbene
which is a weak acid
carbanion
carbocation
radical
carbene
available energy
entropy
gibbs free energy
gibbs energy
enthalpy
in gibbs free energy <0 would mean it is a ___________ reaction
equilibrium
neutral
spontaneous
non-spontaneous
equation for gibbs free energy
ΔG= ΔH-TΔS
ΔG= ΔH+TΔS
ΔH= ΔG-TΔS
ΔG= ΔH-SΔT
enthalpy
total energy
partial energy
disorder of system
available energy
disorder of a system
gibbs free energy
enthalpy
entropy
ΔG >
endergonic
exergonic
equilibrium
exothermic
ΔG <
endergonic
exergonic
equilibrium
exothermic
ΔG = 0
endergonic
exergonic
equilibrium
exothermic
is the study of the energy changes that accompany chemical and physical transformations
thermodynamics
kinetics
study of reaction rates
thermodynamics
kinetics
step by step description of how a reaction happens
mechanics
rate law
the relationship between the concentrations of the reactants and the observed reaction rate
mechanics
rate law
determined experimentally
mechanics
rate law
the number of molecules of that reactant which represent in the rate-determining step
rate law
order
mechanics
exothermic
heat is absorbed
heat is released
-ΔH
+ΔH
endothermic
heat is absorbed
heat is released
-ΔH
+ΔH
what kind of reaction is this
exergonic
endergonic
what kind of reaction is this
exergonic
endergonic
minimum kinetic energy needed to react
Ea
Eact
Eacc
E
which of the following has p-orbital
carbanion
free radical
carbocation
carbene
which is the most stable of the following based on stability of carbocation and radicals
secondary
tertiary
primary
methyl
which is the second most stable of the following based on stability of carbocation and radicals
secondary
tertiary
primary
methyl
which is the least stable of the following based on stability of carbocation and radicals
secondary
tertiary
primary
methyl
bond ________ requires energy (+BDE)
dissociation
formation
bond ________ releases energy (-BDE)
dissociation
formation
what kind of BDE of free radical is this
formation of methyl radical
formation of primary radical
formation of secondary radical
formation of tertiary radical
what kind of BDE of free radical is this
formation of methyl radical
formation of primary radical
formation of secondary radical
formation of tertiary radical
what kind of BDE of free radical is this
formation of methyl radical
formation of primary radical
formation of secondary radical
formation of tertiary radical
what kind of BDE of free radical is this
formation of methyl radical
formation of primary radical
formation of secondary radical
formation of tertiary radical
which of the following has trigonal planar geometry
carbocation
free radicals
carbenes
radicals
which of the following has trigonal pyramid geometry
carbocation
free radicals
carbenes
radicals
which of the following has linear or bent geometry
carbocation
free radicals
carbenes
radicals
are nucleophilic and basic
carbocation
free radicals
carbanion
carbene
carbon is neutral
carbocation
free radicals
carbanion
carbene
donation of electron density along the sigma bonds
inductive effect
hyperconjugation
overlap of sigma bonding orbitals with empty p orbital
inductive effect
hyperconjugation
more highly substituted carbocations are ____ stable
less
more
electron deficient
carbocations
carbanions
radicals
carbenes
electrophilic strong acids
carbocations
carbanions
radicals
carbenes
nucleophilic strong bases
carbocations
carbanions
radicals
carbenes
both nucleophilic and electrophilic
carbocations
carbanions
radicals
carbenes
the highest point in the graph
activation energy
reactive intermediates
rate determining step
transition state
the energy difference between the reactants and the transition state.
activation energy
reactive intermediates
rate determining step
transition state
carbocation, carbanion, free radicals, carbenes
activation energy
reactive intermediates
rate determining step
transition state
____ reactions have transition states, ____ exceptions
all; some
some; no
some; some
all; no
which is used in organic chemistry
ΔH
ΔG
which is used in biochemistry
ΔH
ΔG
lowest point in a graph
transition
intermediate
The reaction step with the highest Ea will be the _______ step and will determine the rate at which the reaction proceeds
fastest
slowest
transition state resembles the product
endothermic
exothermic
transition state resembles the reactant
endothermic
exothermic
first step in free radical chain reaction
initiation
termination
propagation
second step in free radical chain reaction
initiation
termination
propagation
last step in free radical chain reaction
initiation
termination
propagation
The intermediate reacts with a stable molecule to produce another reactive intermediate (and a product molecule).
initiation
termination
propagation
are side reactions that destroy the reactive intermediate.
initiation
termination
propagation
generates a radical intermediate
initiation
termination
propagation
An electron-rich molecule or ion that is capable of donating a pair of electrons
nucelophile
electrophile
An electron-deficient molecule or ion that is capable of accepting a pair of electrons
nucleophile
electrophile
The ability of an atom or molecule to distribute its electron density unevenly in response to external influences
polarizability
polarization
polarized
polar
