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What is an organic molecule?
carbon-based molecules
there are two types of electrons in atoms name them and tell how are they different
core and valence electrons
valence electrons are found on outer energetic layer=on them do chemichal reactions depend
which particle makes up most of the volume in atom?
electrons(cloud) do = imporntant for molecules formation
what is the electronegativity trend across the periodic table?
more right and more up electronegativity increases
what is an alternative name for energy level?
shell
what is an alternative name for shell in atoms?
energy leve
what are core electrons?
electrons in the inner shell(s)
what are calence electrons?
electrons in the outer shell
by which 3 rules can ground -state electron configuration be built?
1. Aufbau principle: An electron goes into the atomic orbital with the lowest energy.
2. Pauli exclusion principle: No more than two electrons can be in an atomic orbital.
3. Hund's rule: An electron goes into an empty degenerate orbital rather than pairing up
define Aufbau principle
An electron goes into the atomic orbital with the lowest energy.
define Pauli exclusion principle
No more than two electrons can be in an atomic orbital.
define Hund's rule
An electron goes into an empty degenerate orbital rather than pairing up.
what are degenerate orbitals?
Degenerate orbitals are orbitals that have the same energy. They are different (they may display differently in space around the nucleus) but they are associated to the same energy.
define octet rule
atom is most stable(energetically favorable)when outer shell is filled or empty
what dipole moment of the bond tells us about bond polarity?
Greater dipole moment = more polar
how to calculate a formal charge?
formal
charge= # of valence electrons -(# of lone-pair
electrons + # of bonds)
Name steps of drawing molecule in Levis structure
1. Determine the total(if minus or plus is present in molecule it means more or less electrons correspondingly) number of valence electrons
2. Distribute the atoms
3. Form bonds and fill octets with lone pairs
4. Check for formal charges
what is C hybridization when it has 4 bonds?what is its geometry and angle?
sp3,tetrahedral,angle=109.5
what is hybridization of C when it has one double and two single bonds?what is its geometry and angle?
sp2,trigonal planar,angle>120
what is hybridization of C when it has one triple and one single bond?what is its geometry and angle?
sp,linear angle=180
what is hybridization of O when it has two single bonds?what is its geometry and angle?
sp3,bent >109.5
what is hybridization of O when it has one double bond?what is its geometry and angle?
sp2,linear angle=180
what is hybridization of N when it has three single bonds?what is its geometry and angle?
sp3,tetrahedral(with lone pair taking one angle) angle>109.5
what is hybridization of N when it has one double and two single bonds?what is its geometry and angle?
sp2 trigonal planar(?)
what is hybridization of N when it has one triple bond?what is its geometry and angle?
sp just nitrogen
what is the shape of an s orbital?
a sphere
what is the shape of a p orbital?
dumbbells(гантели) in 3 planes(x,y,z)
by which two orbitals is σ (sigma) bond formed?
by two s orbitals
what kind of bond will two s orbitals form?
σ bond
what is VSEPR(Valence-shell electron repulsion model )
Bonding electrons and lone-pair electrons around an
atom are positioned as far apart as possible!
what kind of bond do two p orbitals form?
π (pi) bond
with which orbitals can π bond be formed?
with two p orbitals
how to distinguish cis and trans?
when there is a C=C bond the groups with the highest priority on one side is cis
on the opposite sede is trans
how to distinguish E and Z iizomers?
Z=zamen/samen =highest priority on the one side
E =on diff sides
how to distinguish R and S iizomers on asymm.center?
from highest to lowest priority turning to lower and lower
R rotation clockvise
S=counterclockvise
how to rotate molecule for better R and S configuration?
how to distinguish cis & trans,Z & E isomers?
in cis and Z groups with the highest priority are on one side of the molecule
where can Φ angle be found in a peptide bond?
α-N
(since protein starts from N terminus and goes to C terminus by convention ,then Ф on the left, Ψon the right side of α carbon)
(alpha carbon to N connection)(alpha carbon is the carbon which is attached to amine group and Carboxylic group)
where can Ψ angle be found in a peptide bond?
α-C
(since protein starts from N terminus and goes to C terminus by convention ,then Ф on the left, Ψon the right side of α carbon)
(alpha carbon to Carboxyl group connection)(alpha carbon is the carbon which is attached to amine group and Carboxylic group)
what will happen to the proton if pKa is higher than pH?
H+ remains
what will happen ito the proton if pKa is lower than pH?
H+ will be removed
what will happen if pH is higher than pKa?
H+ will be removed
what will happen if pH is lower than pKa?
proton stays
what is a A nucleophile?
something that has a negative charge(-) or a lone pair.
free e pair,donates e pair
better e- accomodation=weaker nucleophile
what is An electrophile?
something that hasa positive charge(+),
a partial positive charge,
or an incomplete octet.(has a free orbital to accept electons)
how to find a rate determining step for sure?
it has the highest transition state
give an equation of a reaction rate
Rate=k{product}
Rate=k{product1}{product2}
how do curved arrows indicate movement of electrons?
a curved arrow indicates a movement of an electron pair,half arrow indicates movement of a single electron
what are rules concerning use of arrows to show a movement of e-/e- pairs?
e- always moves towards positive charge
Octet rule=if 5th thing attaches to a carbon then one thing has to leave
Arrows go according to the electron flow. So an arrow goes from negatively charged atom and/ot point out to the positively charged one
Arrows show the movement of electrons, not atoms
Arrow heads always point to an atom or a bond. Never to space.
Arrows always start at electron source (bond, electron pair), never at an atom
what are rules for drawing curwed arrows?
Arrows go according to the electron flow. So an arrow goes from negatively charged atom and/ot point out to the positively charged one
Arrows show the movement of electrons, not atoms
Arrow heads always point to an atom or a bond. Never to space.
Arrows always start at electron source (bond, electron pair), never at an atom
what does thermodynamics looks at?what does it tells us?
difference in energy between a reactant and a product
It tells us:
what is more energeticaly stable
how good is the reaction in terms how much of a product is formed
what does kinetics looks at?what does it tells us?
activation energy
how unwillingly something rqcts
how fast the reaction happen
do they and how do rate constant and reaction rate change if concentration of reactants changes?
Rate Constant always stays the same
Reaction rate changes
(if there are two reactants and we decrease concentration of one of them=reaction rate decreases)
what atoms are parts of a planar double bond system?
carbons which are connected to a double bond & atoms connected to them
what is a Reaction coordinate diagram?
energy diagram
describe/define transition state
higher in energy than a reactant and a product
bonds are partially broken and partially formed
state Le Chatelier principle
if an equilibrium is disturbed,the system will adjust to offset the disturbance and maintain the equilibrium.
how can we use Le Chatelier principle to increase the number of reaction products?
Add more of one of the reactants
Remove the product in another reaction (or physical process
A + B to C to D
give an equation for Gibbs free energy and annotate what stands for what
ΔG=ΔH-TΔS
ΔH=change in enthalpe
T=change in temperature
ΔS=entropy
when can ΔS be ignored?
the temperature is low AND
The enthalpic therm is not close to zero AND
We expect the So to be small
This gives a good estimation if Go is favorable, but not of exact value
what value does ΔG has to be for a reaction to occur?
negative
how to find ΔH of the reaction?
Look at the dissociacion enthalpies (DH) of bonds being broken and formed
ΔH(broken during reaction) - ΔH(being formed)
what determines rate of the reaction?
(number of collisions per unit of time)x(fraction of collisions with sufficient energy to break/form bonds)x(fraction with proper geometry=molecules do have to hit each other with a correct sight)
which configuration E or Z is lower in energy?what is the reason behind it?
E
orbitals overlap a bit in cis isomer while they don't in trans
how to arrange carbons around carbons which are connected by double bond so it is more energetically favorable?
attach as many other carbons to carbons connected by a double bond as much as possible
define Thermodynamic stability
indicated by G°. If G° is negative, then the product is
Thermodynamically stable compared with the reactant; if G° is positive, then the product
is thermodynamically unstable compared with the reactant.
definne Kinetic stability
indicated by G‡. If G‡ is large, then the reactant is kinetically stable
because it reacts slowly. If G‡ is small, then the reactant is kinetically unstable—it reacts
rapidly. Similarly, if G‡ for the reverse reaction is large, then the product is kinetically
stable, but if it is small, then the product is kinetically unstable.
how can we improve a reaction rate?
Increasing the concentration increases the rate
Increasing the temperature increases the rate.
Adding a catalyst increases the rate.(lowers activation energy by making an intermediate more stable)
what is Boltzmann distribuion show?
it compares number of particles,ther energy and how much particles have sufficient energy for a succesfull collision for two different temperatures
distinguish between enantiomers,diasteomeres and stereoisomers
what is an angle between atoms jn tetrahedral molecules?
109.5
how is Keuke drawing different from Lewis?and in N with 3 bonds?
Keuke draws with perspective.In N 107.3
what is relation between bond length and its strenth?
shorter the bond=stronger
the stronger s character then ... the bond
shorter and stronger
distinguish localized and delocalized electrons
localized electrons belong to 1 atom or are shared by 2 atoms
delocalized electrons are shared by 3 or more atoms
distinguish resonance contributors and resonance hybrids
resonance contributors are approx. structures with localized e
resonance hybrids are structures with delocalized e- shown.
what is a requirment for delocalization?
p-orbitals must lie in the same plane and overlap for delocalization.
rules for drawing resonance structures and hybrids
1. Only electrons move, atoms never move!
2. Only π-electrons and lone pair electrons move!
3. Move electrons always to an sp2 or sp hybridized atom!
4. The number of electrons in the molecule does not change!
5. Do never break a σ-bond!
lone pair e- can move to an sp2 carbon but not to a sp3 carbon
where can lone pair e- move in resonance structures?
lone pair e- can move to an sp2 carbon but not to a sp3 carbon
which chair configuration is more stable?
distinguish enantiomers, diastereomers, and meso compounds
if a group points towards you how will it point on the chair configuration?
it will point up
what will happen to a geometry of a compound during sn2 substion reaction?
int will invert
define apo enzyme
enzyme without a cofactor
define holo enzyme
apo enzyme with a cofactor
what is active site of an enzyme?
a site to which substrate(s) bind
which bond is longer sp2-sp2 or sp3-sp2
sp3-sp2 since less s character=longer bond
prostetic group
tightly bound to enzyme cofactor
holoenzyme
apo enzyme +cofactor
coenzyme
losely bound cofactor
induced fit model
when substrate binds to an enzyme and enzyme chages its shape to better interract with a substrate
to have a better binding
burst phase(of a reaction)
rapid release of a product in the very beginning of the reaction(initially all of enzymes are occupied
(first phase)
catalytic triad
A catalytic triad is a set of three coordinated amino acids that can be found in the active site of some enzymes.
what does kinase enzyme do?
it phosphorelates specific compounds making them more negatively charges and often reactive
in which direction proteins go?
from N to C
basicity trnd in periodic table
bacisity increases up and right in periodic table
how to determine the strongest base in the molecule
further from electronegative parts=stronger base
meso compounds
same molecules
in terms of bacisity which are good leaving groups?
weak bases
what is a good nucleophile?
negatively charged molecule