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types of organic reactions |
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Definition
-addition -elimination -substitution -rearrangement |
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occur when 2 reactants add to form one product, with no atoms left over
A + B --> AB |
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occur when a single reactant splits into 2 products
AB --> A + B |
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occur when 2 reactants exchange parts to yield 2 new products
AB + CD --> AD + CB |
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occur when a single product undergoes a rearrangement of bonds to yield an isomeric product
ABCD --> DBCA |
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Definition
describes the bonds broken and formed in a chemical reaction, and accounts for all reactants and products |
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types of bond breaking in chemical reactions |
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symmetrical bond breakinbg such that 1 electron remains with each fragment |
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heterolytic bond breaking |
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unsymmetrical bond breaking such that both electrons remain with one fragment and the other fragment has a vacant orbital |
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types of bond formation in chemical reactions |
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Definition
-symmetrical -unsymmetrical |
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symmetrical bond formation |
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Definition
each reactant contributes 1 electron to a covalent bond |
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depiction of symmetrical bond formation |
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Definition
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unsymmetrical bond formation |
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Definition
both electrons in a covalent bond come from 1 reactant |
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depiction of unsymmetrical bond formation |
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Definition
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Definition
-radical -polar -pericyclic |
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Definition
involve symmetrical bond breaking and bond formation |
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Definition
involve unsymmetrical bond breaking and bond formation |
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Definition
reactant that contains an atom with an unpaired electron |
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why radicals are highly reactive |
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Definition
because they contain an atom with an unpaired electron |
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substitution reaction that involves a radical |
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Definition
occurs when a radical abstracts an atom and a bonding electron from another molecule |
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addition reaction that involves a radical |
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Definition
occurs when a radical adds to a double bond |
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steps in a radical reaction |
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Definition
-initiation step -propagation steps -termination step |
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Definition
produces radicals by the symmetrical clevage of a bond |
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chain reaction where a radical abstracts an atom to produce a new radical and a stable molecule |
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how bond breaking and formation works in radical reactions |
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Definition
all bonds are formed and broken by reactions of species with odd numbers of electrons |
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Term
some characteristics of polar reactions |
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Definition
-they occur as a result of differences in bond polarities within molecules -electron-rich sites in 1 molecule react with electron-poor sites in another molecule -the movement of electron pairs is shown by curved, fullheaded arrows -the reacting species are nucleophiles and electrophiles -many polar reactions can be explained in terms of acid-base reactions |
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polar reactions occur as a result of... |
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Definition
differences in bond polarities within molecules |
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the polarities within polar molecules are usually due to... |
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Definition
electronegativity differences between atoms |
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electronegativity differences may also be due to... |
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Definition
-interactions of functional groups with solvents -interactions of functional groups with Lewis acids or bases |
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Term
if there's no real electronegativity difference between atoms in a molecule, how can that bond behave as a polar bond? |
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Definition
some bonds in which 1 atom is polarizeable may also behave as polar bonds |
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Term
the sites that react in polar reactions |
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Definition
the electron-rich sites in one molecule react with the electron-poor sites in another molecule |
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the movement of an electron pair in a polar reaction is shown by... |
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Definition
a curved, fullheaded arrow |
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the reacting spevcies in a polar reaction |
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Definition
-nucleophile -electrophile -some compounds behave as both nucleophiles and electrophiles |
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Definition
compound with electron-rich atom |
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compound with electron-poor atom |
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many polar reactions can be explained in terms of... |
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an example of a polar reaction |
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Definition
addition of HBr to ethylene |
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what type of addition is the addition of HBr to ethylene? |
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Definition
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the behavior of the π electrons in ethylene in the addition of HBr to ethylene |
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Definition
the π electrons in ethylene behave as a nucleophile |
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how the reaction of the addition of HBr to ethylene begins |
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Definition
the attack of the π electrons on the electrophile H+ |
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what happens at the end of the reaction of the addition of HBr to ethylene? |
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Definition
the resulting intermediate carbocation reacts with Br- to form bromoethana |
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rules for using curved arrows in polar reaction mechanisms |
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Definition
-electrons must move from nucleophile to electrophile -nucleophile can be negative or neutral -electrophile can be positive or neutral -the octet rule must be followed |
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how chemical reactions can be expressed as equilibria |
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Definition
all chemical reactions are equilibria that can be expressed by an equilibrium constant (Keq) that shows the ratio of products to reactants |
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what must the energy be for the reaction to proceed as written? |
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Definition
to proceed as written, the energy of the products must be lower than the energy of the reactants |
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the energy change that occurs during a reaction is described by... |
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Definition
ΔG°, the Gibbs free-energy change |
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favorable reaction (spontaneous) |
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Definition
have negative ΔG° and are exothermic |
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unfavorable reaction (nonspontaneous) |
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Definition
have positive ΔG° and are endothermic |
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the relationship between ΔG° and Keq |
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Definition
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enthalpy, which is a measure of the total change in bonding energy during a reaction |
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the reaction is exothermic |
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Definition
the reaction is endothermic |
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entropy, which is a measure of the freedom of motion of a reaction |
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rxn with positive entropy |
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Definition
produces 2 product molecules from 1 reactant molecule |
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rxn with negative entropy |
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Definition
produces 1 product molecule from 2 reactant molecules |
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relationship between ΔG°, ΔH°, and ΔS° |
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Definition
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bond dissociation energy (D) |
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Definition
measures the heat needed to break a bond to produce 2 radical fragments |
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what happens to the strength of bonds in exothermic reactions? |
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Definition
the bonds formed are stronger than the bonds broken |
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what reaction energy diagrams show |
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Definition
the energy changes that occur during a reaction |
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how a reaction energy diagram is set up |
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Definition
vertical axis represents energy changes and horizontal axis represents the progress of the reaction |
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the highest energy species in a reaction |
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Definition
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can a reaction have more than 1 transition state? |
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Definition
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the energy of activation (ΔG‡) |
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Definition
the difference in energy between the reactants and the transition state |
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values of ΔG‡ range from... |
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Definition
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what a reaction can do after reaching the transition state |
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Definition
it can go on to form products or revert to starting material |
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Definition
in a reaction of at least 2 steps, this is the species that lies at the energy minimum between 2 transition states |
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energy of an intermediate |
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Definition
even though it lies between 2 transition states, it is a highg energy species |
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can an intertmediate be isolated? |
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Definition
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the solvents laboratory reactions are carried out in |
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Definition
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the medium biological reactions occur in |
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Definition
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the temperatures laboratory reactions take place in |
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Definition
a wide range of temperatures |
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the temperatures biological reactions take place in |
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Definition
the temperature of the organism, usually within narrow limits |
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the catalyzing in laboratory reactions |
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Definition
uncatalyzed or use simple catalysts |
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the catalyzing in biological reactions |
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Definition
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description of laboratory reagents |
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Definition
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description of biological reagents |
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Definition
involve large, complex coenzymes |
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specificity of biological reactions |
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Definition
they have high specificity for substrate |
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specificity of laboratory reactions |
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Definition
they are relatively nonspecific |
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are atoms w/ vacant orbitals electrophiles or nucleophiles? |
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Definition
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a type of rxn that has a carbocation intermediate |
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Definition
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activation energy vs. speed of rxn |
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Definition
the higher the activation energy, the slower the rxn |
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are pi bonds electrophiles or nucleophiles? |
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Definition
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are aromatic rings electrophiles or nucleophiles? |
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Definition
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the difference between exothermic and exergonic |
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Definition
exothermic = -ΔH° exergonic = -ΔG° |
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the difference between endothermic and endergonic |
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Definition
endothermic = +ΔH° endergonic = +ΔG° |
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location of transition state in energy diagram |
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Definition
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location of intermediate in energy diagram |
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