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Atoms
Smallest particle of an element.
3 subatomic particles:
electrons
protons
neutrons
Isotopes
Atoms of an element that have the same number of protons but different number of neutrons
Radioisotope: An unstable isotope that decays over time
Emitted particle and energy
Valence Electrons
Electrons that occupy the outermost shell of an atom.
Participate in chemical bonding
Atoms move electrons between their valence shells to achieve a full valence shell
H, Li, Be are stable with 2 electrons, while most atoms require 8 electrons for a full valence shell
Ion
Atom or molecule that has become charged due to addition or removal of electrons
Cation
Positive charged ion
Lost electrons
Anion
Negative charged ion
Gained electrons
Ionic Bond
The electrostatic (positive + negative) force of attraction between two oppositely charged ions
Extremely strong
Often readily readily soluble in polar solvents (water)
Covalent Bonds
Sharing one or more pairs of electrons between atoms
Two or more atoms bonded together in this way make a molecule
Bond Polarity
Electronegativity (EN)
The measure of an atoms attraction to shared electrons
Atoms in covalent bonds often don’t share electrons equally
EN values can be compared to determine if a bond is polar or nonpolar
Polar Covalent Bonds
UNEQUAL SHARING of electrons
Difference in EN of atoms bonded is more than of equal to 0.41
Nonpolar Covalent Bonds
EQUAL SHARING of electrons
Difference in EN of atoms bonded is less than or equal to 0.40
Molecule Polarity
Polar bonds have a positive and negative side
May cause molecules may also have a positive and negative side
Higher EN is the negative side
Lower EN is the positive side
Indicated using dipoles
If molecules contain only nonpolar bonds, or if their polar bonds are equally distributed, molecules will be nonpolar
Intermolecular Forces
Attraction between two forces
Dipole-Dipole
Intermolecular force between the negative side dipole of a molecule and the positive dipole of another molecule
London Dispersion Forces
Help determine the physical properties of substances
Melting point
Boiling point
Hardness
Attractive force between particles caused by attraction of the electron on one particle to the p on the other particle and vice versa.
EXIST BETWEEN ALL PARTICLES
Rely on random motion of electrons
Temporary & very weak
The relative strength increases with the surface area of the molecule and the number of electrons contained within it (more electrons and surface area=more LDF strength)
Dehydration Synthesis Reaction
Larger molecule is made from smaller molecules via the removal of water
“Condensation” reaction
When growing, body dehydrates
Hydrolysis Reaction
Water is used to break down larger molecules into smaller
Anabolism
Biochemical reactions that make larger molecules from smaller ones
Catabolism
Biochemical reactions that break down larger molecules into smaller ones
Neutralization Reaction
An acid and a base are combined to make ionic compound (a salt) and water
Water
All cellular processes occur in an aqueous environment
Can form four H-bonds with other water molecules
Heat Capacity
Liquid water only escapes as vapor molecule ONCE enough energy has been provided to break all IMFs surrounding it
Strong IMFs
High melting/boiling point
While most substances become more dense as they get colder, water molecules become less dense, which makes it float
Happens because molecules spread out into a crystalline structure (lattice)
Ice insulate aquatic life in cold weather
Specific Heat Capacity
Energy required to raise the temperature of 1kg of substance by 1C
Cohesion
Attraction of particles within the same substance
Ability to stick to itself
Adhesion
Attraction of particles of different substances
Ability to stick to other things
Curve caused by water adhering to glass
Aqueous Solution
Ion or polar molecule is placed in water and gets surrounded by water molecules in a layer called a Hydration Shell
Ionic crystals split into smaller pieces in water as the water molecules form dipole-ion IMFs with them and form hydration shells
Hydrophobic
Nonpolar molecules DO NOT LIKE WATER
Hydrophilic
Polar molecules LIKE WATER
Ionization and pH
Autoionization of water
Water reacts with itself
2 water molecules can perform the reaction:
H2O + H2O = H3O (hydronium) +OH (hydroxide)
Acids
Compound that make H3O ions more concentrated than OH ions
Have an ionization hydrogen (H that can dissociate, break off)
Sour
Watery
Red
Conductor of electricity
pH of less than 7.0
H3O
Bases
Compound that make OH ions more concentrated than H3O ions
Bitter
Slippery
Blue
Conductor of electricity
pH or more than 7.0
2 ways bases work
Have an ionizable hydroxide that can dissociate (break off)
May remove an H ion from a water molecule
OH
pH
Measurement of concentration of H in a solution
Functional Groups
specific combination if atoms that affect the chemical properties of a molecule
Sites on molecules that reactions take place
Type of functional group + location determines what the molecule does
Most are polar
Increase solubility within the aqueous cellular environment (organic molecules are mostly nonpolar C-H bonds)
Carbon is the main element of most biochemical molecules
Called organic molecules
Bonded with non-metals
Provides 4 possible bonding combinations (4 valence electrons)
Carbon forms cyclic structures (ring shaped)
Alkane
Hydrocarbon carbon-carbon bonds are SINGLE BONDS
Alkene
Hydrocarbon 1+ carbon-carbon DOUBLE BONDS
Alkyne
Hydrocarbon 1+ carbon-carbon TRIPLE BONDS
Aromatic Ring
Cyclic structure with alternating DOUBLE bonds
Aliphatic RIng
Cyclic structure WITHOUT alternating DOUBLE bonds
Hydroxyl
-OH group + C atom
Defining functional groups in ALCOHOL compounds
Carbonyl
C=O group + C atom
Aldehyde
When attached to a C and a H as well
Ketone
When attached to 2 Cs
Carboxyl (acid group)
C atom + COOH group
Found in organic acids (amino acids)
Amino
-NH2 group + C atom
Compounds classified as amines
Found in amino acids
Phosphate
-PO4 group + C atom
Found in biochemical molecules
Genetic material
Sulfhydryl
-SH group + C atom
Used give proteins their shape
Classified as thiols
Carbohydrates (Saccharides)
Most common biological molecules
Cx(H2O)y
High-energy food source (starches, sugars)
Used fro cellular communication (cells have embedded carbohydrates to communicate with nearby cells)
ALL HAVE CARBON RINGS WITH O
Monosaccharides
Formula: CnH2nOn
Can be classified by how many carbons they contain
5+ Carbons can be folded to make ring shape
DOUBLE BONDED O NEEDS TO FIND H
Aldose
An aldehyde monosaccharide
Ketose
A ketone monosaccharide
Anomers
Cyclic isomers with same atomic connectivity, but different 3D arrangements
C1 carbon is called anomeric carbon (with H and OH, next to O)
Alpha or Beta
Look at C1 and CH2OH
If they are going in the same direction, beta
If they are going in opposite directions, alpha
Isomer
Molecule with same chemical formula as another molecule, but different arrangement of atoms
C atoms need to be numbered
Galactosemia
Genetic inability to metabolize galactose
Normal people are able to convert galactose to glucose
People with galactosemia must avoid dairy (dairy is main source of galactose)
Glycosidic Bonds
-C-O-C- linkage between monosaccharides
Results in larger molecule
Naming Glycosidic Bonds
Take alpha or beta (depending on the format)
Add the numbers of the carbon atoms
Add glycosidic bond to end
Lactose Intolerance
Person does not have lactase enzyme
Oligosaccharides
Bonding 2-10 monosaccharides to make a chain
Inulin
Indigestible prebiotic for digestive health
Oligofructose
Prebiotic (plant based food)
In cell membranes act as receptors to help cells communicate
Polysaccharides
Made from bonding many monosaccharides to make a chain
Complex Carbohydrates
Very large polysaccharide containing up to thousands of monosaccharides
Polymer
Large molecule made up of smaller repeating molecules called monomers
Polysaccharide is a polymer of monosaccharide monomers
Glycogen
Glucose storage molecule for many organisms including humans
Found in liver and muscle cells
Glucose Regulation
Primary source of energy for body
Blood-glucose levels controlled by two hormones
Insulin
When blood-glucose is too high
Glucagon
Blood-glucose is too low
Hypoglycemia
Blood-glucose concentration lower than the standard range (less than 60 mg/dL)
Being on a diet
Hyperglycemia
Blood-glucose concentration higher than the standard range (more than 200 mg/dL)
Type 1 Diabetes
Low insulin
Glucose is not converted to glycogen
Type 2 Diabetes
Insulin resistance
Glucose is not converted to glycogen
Cellulose
Tough, insoluble, ingestible fiber
Beta-1,4-glycosidic bonds
Plant-based food
Dietary fiber
Chitin
Beta-1,4-glycosidic bonds
different
Low Carb Diet
Initial weight loss is mostly due to glycogen stores in the liver and muscles being depleted
Less bloating
Dehydration
Fatigue
Loss of muscle tone
Lipids
Nonpolar organic compound normally consisting of C, H, bit of O
Functions of Lipids
Long-term energy storage
Insulation of internal organs
Membrane structure
System-wide messenger molecules (hormones)
Fatty Acids
Hydrocarbon chain with a carboxyl functional group at the end(acidic)
Make fatty acids slightly soluble
Longer the hydrocarbon chain is the less soluble
Saturated Fatty Acids
Hydrocarbon chain has only single bonds, results in the maximum amount of H in the molecule
Long linear carbon chains
Unsaturated Fatty Acids
Hydrocarbon chain contains double or triple between carbons
Bend or linear carbon chains depending in which side of the double bond hydrogen atoms are on
Polyunsaturated Fatty Acids
2 or more double or triple bonds
Cis Fatty Acids
Unsaturated fatty acids that bend because the H atoms are on the same side of the C=C bond
Trans Fatty Acids
Unsaturated fatty acids that are linear because the h atoms are on opposite sides of the C=C bond
Hydrogenation
Additions of H atoms to unsaturated fatty acids
Partial hydrogenation can turn a cis fatty acid into a trans fatty acid
Full hydrogenation will saturate unsaturated fatty acids
Fats
Lipids made from the dehydration synthesis reaction between glycerol and up to 3 fatty acids
Make water
Ester Linkage
-COOC- group that connects a fatty acid to a glycerol in a fat molecule
Monoglyceride
Fat made with glycerol and 1 fatty acid
Diglyceride
Fat made with glycerol and 2 fatty acids
Triglyceride
Fat made with glycerol and 3 fatty acids
Saturated Fats
Fats that contain only saturated fatty acids
Often solid at room temperature because their linear fatty acids are packed more closely together
Unsaturated Fats
Fats that contain one or more unsaturated fatty acids
Often liquid in room temperature
Oils
weak IMF
Trans Unsaturated Fats
Unhealthy fats
Solids at room temperature because they are linear & densely stack with each other
Essential Fatty Acids
alpha -linolenic acid (omega--3)
Linoleic acid (omega-6)
Effect
Blood clotting
Blood pressure
Brain growth and function
Inflammation
Mood
Behaviour
Phospholipids
A lipid containing a phosphate group
Used to make cell membranes
Have a structure similar to phosphattidyl ethanolamine
Amphipathic
a molecule that contains both a polar (hydrophilic) and nonpolar (hydrophobic) region
Bilayer of the cell membrane provides a barrier that is hydrophilic on the exterior with a hydrophobic interior
Steriods
A lipid with a base framework of 4 carbon rings\
Bile acid
For lipid absorption in the small intestine
Campesterol
Lowers cholesterol absorption in the small intestine
Reactants used to from other organic molecules
Can be hormones
Molecule released into the tissue fluid od an organism that helps regulate its growth or behaviour
Testosterone
Regulates body changes during and after puberty
Progesterone
Regulates the menstrual cycle and pregnancy
Cholesterol
helps cell membranes remain fluid and permeable
Can be converted into vitamin D
2 Forms of Cholesterol
HDL (High-Density Lipoprotein)
Picks up cholesterol around the body and carries it back to the liver for removal from the body
LDL (Lower-Density Lipoprotein)
Too much LDL in blood may lead to build-up on the artery walls and atherosclerosis
Bad cholesterol
Leads to heart attack or stroke
Effects of Steroids
effects
Brain
Sex drive
Aggression
Skin
Growth of facial and body hair
Baldness
Male sex organs
Sperm production
Prostate growth
Erectile function
Muscle
Muscle mass and strength
Bone marrow
Red blood cell production
Bone
Bone density maintenance
Side Effects of Steroids
Side effects
Hair loss
Irritability
Mood swings
Ance
Gynaecomastia
Liver damage
Infertility
Shrinkage of the testicles
Increased cardiovascular risk
Impotence
Low libido
Osteoporosis osteopenia (weak bones)
Waxes
Large lipid often by the bonding of fatty acids to alcohols or carbon rings
Extremely hydrophobic (non-polar)
Soft solids
Cutin
Is produced by plants t form a waterproof barrier on fruits, stems, leaves
Birds secrete waxes to keep feathers dry
Structural component used by bees in their hives
Earwax traps particles that may cause ear infection
Proteins
Large, folded polymer molecule made up of amino acids as its monomers
Structural Proteins
Provide shape and form to a cell or organism structure
Defensive Proteins
Helps fight-off infection
Signal Proteins
Carry messages around an organism
Some hormones