FROM ELEMENTS TO COMPOUNDS

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Chemistry

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101 Terms

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elements
- substances that are pure in their nature
- no contaminants, nothing else is mixed in it
- are composed of a single atom
- not just limited to single elements (i.e. Oxygen [O2] is still an element even if 2 oxygen is involved in the molecule)
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compounds
- pure substances that are composed of elements in definite proportions
- heterogenous mixture of atoms
- contains 2 or more kinds of atoms
- ex: water (H2O -> 2 hydrogen, 1 oxygen = 2 kinds of atoms)
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Dalton's Atomic Theory
Dalton's Atomic Theory
- 1808 school teacher and chemist
- "Each element is made up of particles called atoms"
- atoms of a given element are identical
- chemical reactions involve reorganizations of the atoms - changes in the way they are bound together
- but atoms are not chemically changed
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J.J Thomson's Atomic Model
J.J Thomson's Atomic Model
- 1897, British Physicist
- discovered the electron in his cathode ray tube
- plum pudding model of the atom
- there's a big mass of positively charged area/environment where electrons are embedded
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Ernest Rutherford's Atomic Model
Ernest Rutherford's Atomic Model
- 1908
- performed the gold foil experiment
- atom is made up of mostly empty space and contains a positively charged nucleus in the center
- atom is unstable bc of the movement of the electron orbiting around the positively charged nucleus
- no neutrons yet
- protons and electrons are only subatomic particles here
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20th century
20th century
- development of mass spectrophotometers lead to the discovery of neutrons
- neutrons are in nucleus together w/ the protons
- present atomic model where nucleus is composed of protons and neutrons
- electrons surround nucleus
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periodic table of elements
- arrangement of elements by property
- there are trends of several properties in each element
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periods
- atomic size/radius decreases as you move across _____ (from left to right)
- ionization energy increases
- electronegativity increases
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groups
- atomic size/radius increases as you move down ______
- ionization energy decreases
- electronegativity decreases
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periods' atomic size/radius
- decreases as you move across
- number of electrons and protons increase
- increased number of protons increases nuclear charge, pulling the electrons closer to the nucleus
- increased nuclear charge increases its pool
- atom decreases bc of increase in protons and nuclear charge
- composed of positively charged protons and neutral neutrons
- electrons get attracted to nucleus, compressing the atom
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groups' atomic size
- (number of electrons) increase moving down
- more electrons in more principal energy levels
- atom increases
- nucleus can't attract electrons on the outer shell due to inner electrons
- shielding occurs and outer electrons can't feel attracting pull of protons
- repulsions to electrons from both being negatively charged
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ionization energy
- energy needed to overcome reaction of the nuclear charge and remove an electron from gaseous atom
- increases across a period and decreases down a group
- related to atomic size
- outer electrons feel lesser pull from the nucleus bc of the inner electrons
- repulsion and shielding in inner electrons
- bigger atoms are more ready to give up the outer electrons compared to the smaller atoms
- outer electrons of bigger atoms feel less attracted to the nuucleus so they remove more easily
- smaller atoms are more attracted to the nucleus
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electronegativity
- ability of an atom to attract electrons toward itself in a chemical bond
- increases across a period and decreases down a group
- small atomic size/radius = high __________
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electron affinity
- measure if energy is absorbed when an electron is added to a neutral atom to form a negative ion
- most elements have a negative ________ meaning they do not require energy to gain an electron; instead they release energy
- increases across a period and decreases down a group
- small atomic size/radius = high _________
- nucleus' positive charge can accommodate more since there's less shielding and repulsion from inner electrons
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metallic property
- increases down a group
- decreases across a period
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non-metallic property
- decreases down a group
- increases across a period
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how compounds form
- interaction of electrons (outer) of 1 atom and another atom
- attraction between the nucleus and the electrons of another compound being greater than the repulsion of electron-electron and nucleus-nucleus
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chemical bonds
- in any compound formation there are _______ formed
- attractive force that holds 2 atoms together in a more complex unit
- result of interaction between electrons found in the combining atoms
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valence electrons
- electrons in outermost electron shell
- only electrons that interact during chemical bond formation
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Lewis Symbol
chemical symbol of an element surrounded by dots (representation of valence electrons present in atoms of the element)
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valence electron configurations of noble gases
certain arrangements of valence electrons are more stable; __________ are most stable bc noble gases have 8 electrons surrounding them
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octet rule
formation of chemical bonds aims for electrons/elements to have 8 surrounding electrons
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formation of compounds
formation of compounds
atoms of elements lose, gain, or share electrons to produce a "noble-gas electron configuration" for each of the atoms involved
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ionic bonds
bond formed through the transfer of 1 or more electrons from 1 atom/group of atoms to another atom/group of atoms
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ionic compounds
ionic compounds
- always neutral, no net charge
- positive + negative = neutral
- has ionic bonds
- the ratio in which positive and negative ions combine is the ratio that achieves charge neutrality for the resulting compound
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covalent bonds
chemical bond formed through sharing of 1 or more pairs of electrons between 2 atoms
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covalent compound
covalent compound
interaction between 2 or more nonmetals (or other atom involved could be metalloid)
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Valence Shell Electron Pair Repulsion Theory (VSPER Theory)
Valence Shell Electron Pair Repulsion Theory (VSPER Theory)
used to predict the shape of compounds
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shape of molecule/molecular shape
- determined by its bond angles and repulsions between all the electrons present in the valence/outermost shell of the atom
- predicted by assuming the valence electrons repel each other (bc all of them are negatively charged)
- molecule adopts whichever 3D geometry minimized the repulsion
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electron pairs in the valence shell of the central atom
- repel each other and align themselves to minimize repulsion bc repulsion decreases stability of compound
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organization/arrangement in compound
- occurs to minimize repulsion
- lessens interactions between electron pairs (specifically lone pairs)
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lone pair electrons
- take up more space (than the substituents)
- attracted to 1 nucleus but bond pair is shared by 2 nuclei (covalent bond)
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Lewis Structure
using _______, we are able to see which atoms are physically connected to which
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how to know molecular shape of compound
- look at # of lone pairs and # of substituents
- assign a shape where the repulsion of electrons is low
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predicting molecular geometrics
predicting molecular geometrics
1. draw the Lewis Structure
2. count the total number of electron pairs around the central atom
3. arrange the electron pairs such that electron-electron repulsion is at a minimum
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effect of nonbonding electrons and multiple bonds on bond angles
effect of nonbonding electrons and multiple bonds on bond angles
- lone pairs repel more than the bond electrons bc the latter are attracted by 2 nuclei
- bond angle decreases as the number of lone pairs increase
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polarity
- means there are dipoles (a positive and negative end)
- arises from the difference in electronegativity between 2 bonded atoms
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dipole moments
- occurs when atom is electronegative, resulting in a tendency to pull bond electrons towards itself
- once formed, there is partially negative and partially positive ends, hence polar molecules and non-polar molecules
- do not add up to 0 or do not cancel out in polar molecules
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quantum mechanical model of the atom
- most accurate and accepted model of the atom
- derives from the Schrodinger wave equation and deals with probabilities
- electrons do not exist as tiny points inside the atom but instead surround the nucleus in a form resembling a cloud
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probabilities
electrons' position (not the specific position/space of electrons' location)
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electron orbit model
electron orbit model
originally, electrons were thought to orbit around the nucleus in defined paths
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electron cloud model
electron cloud model
- it was discovered that electrons move in waves in a defined space called an electron cloud
- can't pinpoint where an electron is at a specific time
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Heisenberg Uncertainty Principle
- position and momentum of an electron cannot be determined simultaneously w/ absolute accuracy
- if you know the position of an electron you cannot know the momentum of that electron, and vice versa
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wave function
wave function
- helps comprehend the state of a quantum mechanical system
- can be real or imaginary
- no meaning can be assigned to it as it is
- originates from Schrodinger's wave equation
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wave function equation
- compiles the values/variables in order for us to know location or momentum of electron
- cannot really tell us anything about the electron
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square of the function
square of the function
- only quantity that has some meaning according to Max Born
- indicates the probability of finding an electron near a particular point in space at a particular time
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probability density
we cannot entirely say where the location is of an electron
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probability distribution
- intensity of color is used to indicate the probability value near a given point in space
- used after subjecting a specific atom to know where the electron is
- if color in specific area is intense, electrons are most likely there
- color intensity tells us electrons are dense in specific area
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Principal quantum number (n)
- distance from nucleus
- size and energy of orbital
- how close/far is the orbital from the nucleus
- is the number itself in electron configuration
- based on numbers, 1 is closest to nucleus
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Angular momentum quantum number (l)
- shape of orbital
- shape of atomic orbitals (sometimes called a subshell)
- are the letters in electron configuration (s, p, d, f, g)
-> s = spherical
-> p = dumbbell
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Magnetic quantum number (m)
- orientation in space
- axis/portion of space that electrons occupy
- orientation of orbital in space relative to the other orbitals in the atom
-> location/area that electrons occupy
- acquired based on the value of the angular momentum number
-> letters (s, p, d, f) have specific numerical values
-> s = 0, p = 1, d = 2, f = 3
- possible values range from negative angular momentum quantum number to positive angular momentum quantum number
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electron spin (s)
either positive or negative spin
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orientation in space
based on 3 axis (x, y, z)
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orbitals
show where the electrons are
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molecular geometry of water
- molecule is polar bc dipole moments is pointed upwards
- electronegative oxygen pulls electrons towards itself
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water
- universal solvent (dissolves more substances than any other liquid)
- is bent and is a polar molecule due to dipole moment
- follows the "like dissolves like" general rule in terms of solubility (p molecules dissolves p molecules, np molecules dissolves np molecules)
- partial changes in molecule attract parts of other polar molecules to dissolve with them
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Intermolecular Forces of Attraction (IMFA)
- attractive forces between molecules
- called van der Waals forces, named after Dutch scientists Johann van der Waals
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London Dispersion Forces (LDF)
London Dispersion Forces (LDF)
- present in all molecules
- due to the fluctuations in the electron distribution within atoms or molecules
- forces are particularly weak
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Dipole-Dipole Forces
Dipole-Dipole Forces
- attractive forces between polar molecules
- isn't just from instantaneous dipole
- induced by the presence of electronegative atoms
- due to electrical interactions among dipoles on neighboring molecules
- partially positive pole will attract partially negative pole
- repulsion occurs if atoms that are positive-positive poles or negative-negative poles are directed towards each other
- moderately strong bc dipole moment of polar molecules are not instantaneous
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Hydrogen Bonding
- special type of dipole-dipole force
- attractive force between a hydrogen atom of 1 molecule and a highly electronegative atom (O, N, F) of another molecule
- strongest type
- H will attract an electronegative atom to another molecule and it can either be:
-> intermolecular H bonding = between several molecules
-> intramolecular H bonding = within 1 molecule
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application of IMFA
- when molecules have strong intermolecular forces of attraction, they are packed close together; they may also have a relatively high boiling point and/or melting point since it requires a higher amount of energy to break the bond
-> they often exist as a condensed phase (solid or liquid) at room temperature
- when molecules have weak intermolecular forces of attraction, they are far apart from each other, they often exist as gas at room temperature
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solubility
- ability of substance to dissolve in a given amount of solvent at a specified temperature
- when the solute and solvent both exhibit the same intermolecular forces of attraction, they form a solution
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carbohydrates
- polyhydroxy aldehydes and ketones
-> poly = many; hydroxy = OH portion
-> aldehydes and ketones = has a carbonyl group in the molecule
- composed of carbon, hydrogen, and oxygen
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monosaccharides
- simple sugars with 3-7 carbons with a carbonyl group at either terminal C or the C adjacent to it
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aldoses
aldehyde group at C1
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ketoses
ketone group at C2
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disaccharides
- contain 2 monosaccharides linked by a glycosidic bond
- formation proceeds via condensation reaction aka dehydration reaction
-> water molecule is abstracted/removed from the glycosidic bond
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polysaccharides
more than 2 monosaccharides
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cellulose and amylose
- straight chain
- straight linkage of glucose units between carbon 1 and 4 of another glucose unit
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amylopectin and glycogen
- straight chain linkages between carbon 1 and 4 of glucose units
- when it branches out, carbon 1 is connected/bonded to carbon 6 of a glucose unit
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Molisch test
test = for all sugars (steps: dehydration, condensation, and oxidation)
reagent(s) = 1-napthol, ethanol, H2SO4
positive indication = purple interface
- if this test is performed and you see a purple interface, then there is most likely a carbohydrate in your sample
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Benedict's test
test = for reducing sugars
reagent(s) = CuSO4, Na2CO3, sodium citrate
positive indication = brick red-precipitate (if high concentration, green, yellow, or orange precipitates)
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Fehling's test
test = for reducing sugars
reagent(s) = CuSO4, Na2CO3, sodium tartate
positive indication = brick-red precipitate (same as Benedict's Test)
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Osazone formation
test = for identification
reagent(s) = phenylhydrazine
positive indication = yellow crystals
- after formation of crystals, you will subject it to melting point and compare to literature values to know the identity of your carbohydrate
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functions of carbohydrates
- to store and provide energy
- when glucose is further broken down, the energy released by breaking its chemical bonds are sued/stored by the body in the form of glycogen
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proteins
macromolecules comprised of 1 or more long chains of amino acid residues joined together by peptide bonds
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amino acids
basic unit of proteins
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oligopeptides
contain up to about 50 amino acid residues
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polypeptides
contain more than 50 amino acid residues
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2 ends of a peptide
N-terminal and C-terminal
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N-terminal
end with free amino group
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C-terminal
end with carboxyl group
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peptide bond
- bond between amino acid residues
- formation proceeds via dehydration reaction
- lone pair of nitrogen attacks the partially positive carbonyl carbon; a water molecule is abstracted
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primary structure
- the sequence of amino acid comprising the polypeptide chain
- peptide bonds
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secondary structure
- the folding of the polypeptide
- hydrogen bonds between the amino and carboxyl groups of non-adjacent amino acids
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tertiary structure
- the 3D shape of the polypeptide
- interactions between the side chains, hydrogen bonding, disulfide bridges, electrostatic and hydrophobic interactions
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quaternary structure
- inter-chain interactions; formation of subunits
- hydrogen bonds and van der Waals forces between non-polar side chains
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functions of proteins
- they can act as catalysts and hasten chemical reactions; they can transport substances and provide structural support
- many of them function as enzymes (molecules that catalyze or speed up chemical reactions in the body)
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lipids
- consist of a heterogenous group of compounds
- insoluble in water and soluble in non-polar solvents due to the large # of C-C and C-H
- defined on the basis of a physical property and not by presence of functional group
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biological functions of lipids
- store chemical energy in the body
- insulate vital organs
- covering of nerve fibers
- components of cell membrane
- chemical messengers (i.e. hormones)
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saponifiable lipids/hydrolyzable lipids
- can undergo hydrolysis/can hydrolize
- lipids that are converted into smaller molecules by hydrolysis
- contains an ester unit
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tricylglycerols/fats/oils
- esters of fatty acids with glycerol
- main storage form of fatty acids
- contains glycerol and 3 fatty acid chains
- fatty acid attached to glycerol can either be saturated or unsaturated
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waxes
esters of fatty acids with glycerol
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phospholipids
- contains phosphoric acid residue in addition to an alcohol and fatty acids
- major component of cell membranes
- similar to triglyceride but 1 fatty acid is replaced by phosphate group (polar head)
- forms a lipid bilayer; hydrophobic tails are sandwiched between hydrophilic heads
- lipid bilayer acts as barrier to the passage of molecules and ions into and out of the cell
- various protein molecules are embedded in and through the lipid bilayer
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glycerophospholipids
glycerol as a source of alcohol group
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sphingolipid
sphingosine as source of alcohol group
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glycolipids
contain carbohydrate in addition to sphingosine and fatty acid
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non-saponifiable or non-hydrolyzable lipids
- lipids that cannot be broken down into smaller components by aqueous hydrolysis
- examples are steroids and terpenes
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nucleic acids
- polymers also called polynucleotide
-> nucleotide = consists of a nitrogenous base, a pentose sugar, and one or more phosphate groups
-> nucleoside = nucleotide without the phosphate group
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Phosphodiester linkages
what joins nucleotides together between the 5' and 3' OH group of two separate nucleotides