doodlebob
D. Compounds
Compound occurs as result of 2 or more individual elements combining in a fixed ratio
Different properties of individual elements
Formed by chemical reaction
Bonds that hold compounds together
Ionic bonds TRANSFERRED
nonmetal+metal
One or more electrons is transferred from one atom to another
One atom loses electrons (becomes positively charged) while the other gains electrons (becomes negatively charged)
Results from attraction of two oppositely charged ions
Cation has a positive charge
Anion has a negative charge
Cation and anion form to create ionic bond
Covalent bonds SHARED
nonmetal+nonmetal
Molecule consists of 2 or more atoms held together by covalent bonds
Formed when electrons are shared between atoms
In nonpolar covalent bond, electrons are shared equally
In polar covalent bond, electrons are shared unequally
In a single covalent bond, one pair of electrons is shared
Double covalent when 2 pairs are shared, etc.
Structural formula used to represent atoms and bonding
Ex. H-H
Molecular formula abbreviates structural formula
Ex. H2
Electronegativity is an atom’s attraction for the atoms in a covalent bond
The more electronegative an atom, the more strongly it pulls shared electrons toward itself
Hydrogen bonds
Hydrogen atom covalently bonds to one electronegative ato is also attracted to another electronegative atom
In living cells, hydrogen bonds are usually oxygen or other nitrogen atoms
Van der Waals Interactions
Weakest
If electrons are distributed asymmetrically in molecules or atoms, they can result in “hot spots” of positive or negative charge
Attractions between molecules that are close together as a result of these charges
How geckos climb
E. Water: The Versatile Molecule
In water, electrons are not shared equally in the bonds between hydrogen and oxygen
Hydrogen atoms have a partial positive charge while oxygen atoms has a partial negative charge
Water is polar
Hydrogen bonds
Weak attractions that result of water’s polarity
Positive end of another polar molecule attracted to oxygen negative charge, and vice versa with the hydrogen end
Hydrogen atom covalently bonded to one electronegative atom is also attracted to another electronegative atom
Weak Individually, but strong on a larger scale
hydrogen bond= water + water
Lends watermany special properties
Cohesion
Tendency for water to stick to water
Important during transpiration
Water evaporates, pulls other water molecules with it, pulling all the way down from leaves to roots
Adhesion
Tendency of water to stick to other substances
Cohesion + Adhesion = capillary action
Allows water to flow up roots/trunks/branches of trees in thin vessels
Surface tension
Results from cohesion of water molecules
Ex. water striders can sit on top of water without sinking
High heat capacity
Heat CApacity=ability of a substance to resist temperature changes
Keeps ocean temperatures stable
Allows organisms to keep constant body temperature, since most life forms are mostly made up of water
Heat is absorbed when hydrogen bonds break, released when hydrogen bonds form
High heat of vaporization
Heat a liquid must absorb for 1g to be converted to gas
Evaporative cooling
As a liquid evaporates, its remaining surface cools
How sweat works to cool body down
Expansion on freezing
Lattice structure of ice causes water to expand on freezing
Allows ice to float on top of lakes in winter
Animal life can live beneath ice
Versatility as a solvent
Solution is a liquid that is a homogenous mix of substances
Solvent is the dissolving agent of a solution
Solute is the substance that is dissolved
Aqueous solution is one where water is the solvent
Polarity of water allows it to be a versatile solvent
Can form hydrogen bonds easily
Hydrophobic substances do not dissolve in water, but hydrophilic ones will
Carbohydrates
Contain carbon, hydrogen, and oxygen in a 1:2:1 ratio
Monosaccharides
Most common are glucose and fructose
Glucose
Most abundant
Part of food humans eat
Made by plants during photosynthesis
Broken down to release energy
Fructose
Common sugar in fruits
Can be depicted as either straight or rings
6 carbon-sugars
Formula: C6H12O6
Disaccharides
1 monosaccharide+1 monosaccharide=1 Disaccharide
Formed by dehydration synthesis
Aka condensation
Hydrogen (-H) from one sugar combines with hydroxyl group (-OH) of another sugar molecule to create water as byproduct
Bond is called glycosidic linkage
Broken apart by hydrolysis
Reverse of dehydration
Water is used to break apart glycosidic linkage
Polysaccharides
Repeated units of monosaccharides
Most common
Starch
Stores sugar in plants
Made up of alpha-glucose molecules
Cellulose
Made up of ß-glucose molecules
Chitin
Structural molecule in walls of fungi/arthropod exoskeletons
Used as surgical thread since it breaks down in body
Glycogen
Stores sugar in animals
Proteins
Amino acids=monomer of proteins
20 kinds of naturally occurring amino acids
Contain:
Carbon
Hydrogen
Oxygen
Nitrogen
4 parts of an amino acid centered around a central carbon
Amino group (-NH2)
Carboxyl group (-COOH)
Hydrogen
R group
Aka side chain
Interchangeable
Vary in composition, polarity, charge, shape depending on specific side chain
Polar R groups point outward, hydrophobic R groups point inward
Polypeptides
Amino acid + amino acid= dipeptide
Formed by dehydration synthesis
Bond is called a peptide bond
Multiple amino acids= polypeptide
Once a polypeptide chain twists and folds on itself, it forms a 3D structure called a protein
Higher protein structure (4 levels total)
Primary structure
Linear sequence of amino acids
Covalent (peptide) bonds
Secondary structure
Protein beings to twist--2 options
Forms a coil (alpha-helix)
Zigzagging pattern (known as beta-pleated sheets)
Shape depends on R-group
Formed by amino acids that interact with other amino acids closeby in the primary structure
Hydrogen bonds between carbonyl and amino group
Interactions between amino and carboxyl groups of protein backbone
After secondary structure forms, formerly distant amino acids are now closeby--tertiary structure can form
Tertiary structure
Can be both alpha and beta helix/sheets within structure
Covalent disulfide bridge often stabilizes structure
Bonds between R groups
Hydrogen bonds
Ionic bonds
Disulfide bridges
Hydrophobic interactions
Quaternary structure
Several different polypeptide chains sometimes interact with each other
Same bonds as above, but between peptide chains rather than between R groups
Mistakes in structure can denature a protein
Change of shape=change of function
Ex. pH or heat can denature protein
Protein folding can involve chaperone proteins (chaperonins)
Help protein fold properly
Make process more efficient
8 kinds of Proteins | |
Name | Function |
Enzymatic | Selective acceleration of chemical reactions |
Defensive | Protection against disease |
storage | Storage of amino acids |
transport | Transport of substances |
hormonal | Coordination of organism’s biological activities |
receptor | Response of cell to chemical stimuli |
contractile/motor | movement |
Structural | support |
Lipids
Like carbs, consist of carbon, hydrogen and oxygen, but not in a fixed ratio
Do not form polymers
Little-no affinity for water
Hydrophobic due to nonpolar covalent bonds of hydrocarbon
Common examples:
Triglycerides
Glycerol molecule+3 fatty acid chains attached
Fatty acid chain is mostly a long chain of carbons where each carbon is covered in hydrogen; One end of the chain has a carboxyl group (-COOH)
Vary in length and #/location(s) of double bonds
Glycerol is a 3-carbon alcohol with a hydroxyl group attached to each carbon
Fats separate from water because water forms hydrogen bonds with itself while excluding the fats
In order to be made, each of the carboxyl groups of the 3 fatty acids must react with one of the 3 hydroxyl groups of the glycerol molecule via dehydration synthesis
bond=ester linkage
Saturated fatty acid
No double bond
Carbon chain completely filled (“saturated”) with hydrogen
Usually solid at room temp.
Unsaturated fatty acid
Double bond along carbon chain, causing a bend
Bend allows triglyceride to become LESS dense, making it liquid at room temperature
Polyunsaturated fatty acid has multiple double bonds within the fatty acid, causing many bends
Phospholipids
2 fatty acid “tails” + 1 negatively charged phosphate “head”
Tails are hydrophobic, while head is hydrophilic (negative charge on head attracts polar water)
Amphipathic molecule (molecule that is both polar and nonpolar)
In water, phospholipids self-assemble into a “bilayer arrangement”
Hydrophobic tails face towards interior
Found in cell membranes
Steroids
Cholesterol
4-ringed molecule dispersed throughout membrane
Maintains membrane stability
Increases membrane fluidity at lower temperatures by disrupting close packing
Decreases fluidity at high temperatures through its constant movement
Nucleic Acids
Contain carbon, hydrogen, oxygen, nitrogen, and phosphorous
Structure
Nitrogenous base
Pentose sugar
Phosphate group
Portion of nucleotide w/o phosphate group is called nucleoside
Store, transmit, and help expres hereditary information
monomer=nucleotides
Amino acid sequence of a polypeptide is programmed by a unit of inheritance called a gene
Made up of DNA
Deoxyribonucleic acid (DNA)
sugar=deoxyribose
Contains genetic/hereditary information
Provides directions for its own replication
Directs synthesis of messenger RNA (mRNA), and through mRNA, controls protein synthesis
Occurs on ribosomes
Ribonucleic acid (RNA)
sugar=ribose
Essential for protein synthesis
2 families of nitrogenous bases
Pyrimidines
Single 6-membered ring
Ex.
Cytosine
Thymine (only DNA
Uracil (only RNA)
Purines
6-membered ring fused to a 5-membered ring
Ex.
Adenine
Guanine
Nucleotide Polymers
Nucleotide polymers linked together to build a polynucleotide
Adjacent nucleotides are joined by covalent bonds that form between the -OH group on the 3’ carbon of one nucleotide and the phosphate on the 5’ carbon on the next
Links create a backbone of sugar-phosphate units with nitrogenous bases as appendages
RNA molecules usually exist as single polypeptide chains
DNA molecules have 2 polynucleotides spiraling around an imaginary axis, forming a double helix
Two backbones run in opposite 5’→3’ directions from each other (antiparallel)
One DNA molecule contains many genes
Nitrogenous bases pair up and form hydrogen bonds
Adenine-Thymine
Guanine-Cytosine
Complementary base pairing
In RNA, thymine is replaced by uracil, so A and U pair
Macromolecule | Monomer | Polymer | Linkage Bond |
Carbohydrates | Monosaccharide (ex. Glucose) | Polysaccharide (ex. Starch, glycogen, cellulose) | Glycosidic linkage |
Proteins | Amino Acid (Ex. Glycine) | Polypeptide (ex. actin) | Peptide bond |
Nucleic Acids | Nucleotides (ex. Adenine, thymine, guanine, cytosine) | DNA or RNA | Sugar-phosphate phosphodiester bonds |
Lipids | Not a true polymer, but often contains chains of carbons with hydrogens | Triglycerides, Phospholipids, cholesterol | Ester bonds |
F. Origins of the Earth
Alexander Oparin and J. B. S. Haldane proposed that the primitive atmosphere contained the following gases:
Methane (CH4)
Ammonia (NH3)
Hydrogen (H2)
Water (H2O)
No free oxygen (O2)
No oxidation/reduction
Rocks do not release oxygen through weathering
Gases collided, producing chemical reactions that eventually led to the organic molecules we know today
Substantial support until 1953
1953, Stanley Miller and Harold Urey simulated the conditions of primitive Earth in a lab,
Put theoried gases into flask, struck them with electrical charges to simulate lightning, and organic compounds similar to amino acids appeared
Current theory of the origin of life suggests 4 main stages
1. Formation of amino acids
2. Monomers form polymers
3. Enclosure of small organic molecules into larger ones
4. Self-replicating molecules that can direct synthesis of other organic substances
Energy sources for early organic synthesis
Lightning
Volcanic eruptions
RNA world hypothesis
Original life-forms were simple molecules of RNA
RNA not restricted to double helix
RNA capable of replicating and passing genes
Complex organic compounds must have formed via dehydration synthesis
Organic compounds then used as food by cells
Simple cells evolved into complex cells
D. Compounds
Compound occurs as result of 2 or more individual elements combining in a fixed ratio
Different properties of individual elements
Formed by chemical reaction
Bonds that hold compounds together
Ionic bonds TRANSFERRED
nonmetal+metal
One or more electrons is transferred from one atom to another
One atom loses electrons (becomes positively charged) while the other gains electrons (becomes negatively charged)
Results from attraction of two oppositely charged ions
Cation has a positive charge
Anion has a negative charge
Cation and anion form to create ionic bond
Covalent bonds SHARED
nonmetal+nonmetal
Molecule consists of 2 or more atoms held together by covalent bonds
Formed when electrons are shared between atoms
In nonpolar covalent bond, electrons are shared equally
In polar covalent bond, electrons are shared unequally
In a single covalent bond, one pair of electrons is shared
Double covalent when 2 pairs are shared, etc.
Structural formula used to represent atoms and bonding
Ex. H-H
Molecular formula abbreviates structural formula
Ex. H2
Electronegativity is an atom’s attraction for the atoms in a covalent bond
The more electronegative an atom, the more strongly it pulls shared electrons toward itself
Hydrogen bonds
Hydrogen atom covalently bonds to one electronegative ato is also attracted to another electronegative atom
In living cells, hydrogen bonds are usually oxygen or other nitrogen atoms
Van der Waals Interactions
Weakest
If electrons are distributed asymmetrically in molecules or atoms, they can result in “hot spots” of positive or negative charge
Attractions between molecules that are close together as a result of these charges
How geckos climb
E. Water: The Versatile Molecule
In water, electrons are not shared equally in the bonds between hydrogen and oxygen
Hydrogen atoms have a partial positive charge while oxygen atoms has a partial negative charge
Water is polar
Hydrogen bonds
Weak attractions that result of water’s polarity
Positive end of another polar molecule attracted to oxygen negative charge, and vice versa with the hydrogen end
Hydrogen atom covalently bonded to one electronegative atom is also attracted to another electronegative atom
Weak Individually, but strong on a larger scale
hydrogen bond= water + water
Lends watermany special properties
Cohesion
Tendency for water to stick to water
Important during transpiration
Water evaporates, pulls other water molecules with it, pulling all the way down from leaves to roots
Adhesion
Tendency of water to stick to other substances
Cohesion + Adhesion = capillary action
Allows water to flow up roots/trunks/branches of trees in thin vessels
Surface tension
Results from cohesion of water molecules
Ex. water striders can sit on top of water without sinking
High heat capacity
Heat CApacity=ability of a substance to resist temperature changes
Keeps ocean temperatures stable
Allows organisms to keep constant body temperature, since most life forms are mostly made up of water
Heat is absorbed when hydrogen bonds break, released when hydrogen bonds form
High heat of vaporization
Heat a liquid must absorb for 1g to be converted to gas
Evaporative cooling
As a liquid evaporates, its remaining surface cools
How sweat works to cool body down
Expansion on freezing
Lattice structure of ice causes water to expand on freezing
Allows ice to float on top of lakes in winter
Animal life can live beneath ice
Versatility as a solvent
Solution is a liquid that is a homogenous mix of substances
Solvent is the dissolving agent of a solution
Solute is the substance that is dissolved
Aqueous solution is one where water is the solvent
Polarity of water allows it to be a versatile solvent
Can form hydrogen bonds easily
Hydrophobic substances do not dissolve in water, but hydrophilic ones will
Carbohydrates
Contain carbon, hydrogen, and oxygen in a 1:2:1 ratio
Monosaccharides
Most common are glucose and fructose
Glucose
Most abundant
Part of food humans eat
Made by plants during photosynthesis
Broken down to release energy
Fructose
Common sugar in fruits
Can be depicted as either straight or rings
6 carbon-sugars
Formula: C6H12O6
Disaccharides
1 monosaccharide+1 monosaccharide=1 Disaccharide
Formed by dehydration synthesis
Aka condensation
Hydrogen (-H) from one sugar combines with hydroxyl group (-OH) of another sugar molecule to create water as byproduct
Bond is called glycosidic linkage
Broken apart by hydrolysis
Reverse of dehydration
Water is used to break apart glycosidic linkage
Polysaccharides
Repeated units of monosaccharides
Most common
Starch
Stores sugar in plants
Made up of alpha-glucose molecules
Cellulose
Made up of ß-glucose molecules
Chitin
Structural molecule in walls of fungi/arthropod exoskeletons
Used as surgical thread since it breaks down in body
Glycogen
Stores sugar in animals
Proteins
Amino acids=monomer of proteins
20 kinds of naturally occurring amino acids
Contain:
Carbon
Hydrogen
Oxygen
Nitrogen
4 parts of an amino acid centered around a central carbon
Amino group (-NH2)
Carboxyl group (-COOH)
Hydrogen
R group
Aka side chain
Interchangeable
Vary in composition, polarity, charge, shape depending on specific side chain
Polar R groups point outward, hydrophobic R groups point inward
Polypeptides
Amino acid + amino acid= dipeptide
Formed by dehydration synthesis
Bond is called a peptide bond
Multiple amino acids= polypeptide
Once a polypeptide chain twists and folds on itself, it forms a 3D structure called a protein
Higher protein structure (4 levels total)
Primary structure
Linear sequence of amino acids
Covalent (peptide) bonds
Secondary structure
Protein beings to twist--2 options
Forms a coil (alpha-helix)
Zigzagging pattern (known as beta-pleated sheets)
Shape depends on R-group
Formed by amino acids that interact with other amino acids closeby in the primary structure
Hydrogen bonds between carbonyl and amino group
Interactions between amino and carboxyl groups of protein backbone
After secondary structure forms, formerly distant amino acids are now closeby--tertiary structure can form
Tertiary structure
Can be both alpha and beta helix/sheets within structure
Covalent disulfide bridge often stabilizes structure
Bonds between R groups
Hydrogen bonds
Ionic bonds
Disulfide bridges
Hydrophobic interactions
Quaternary structure
Several different polypeptide chains sometimes interact with each other
Same bonds as above, but between peptide chains rather than between R groups
Mistakes in structure can denature a protein
Change of shape=change of function
Ex. pH or heat can denature protein
Protein folding can involve chaperone proteins (chaperonins)
Help protein fold properly
Make process more efficient
8 kinds of Proteins | |
Name | Function |
Enzymatic | Selective acceleration of chemical reactions |
Defensive | Protection against disease |
storage | Storage of amino acids |
transport | Transport of substances |
hormonal | Coordination of organism’s biological activities |
receptor | Response of cell to chemical stimuli |
contractile/motor | movement |
Structural | support |
Lipids
Like carbs, consist of carbon, hydrogen and oxygen, but not in a fixed ratio
Do not form polymers
Little-no affinity for water
Hydrophobic due to nonpolar covalent bonds of hydrocarbon
Common examples:
Triglycerides
Glycerol molecule+3 fatty acid chains attached
Fatty acid chain is mostly a long chain of carbons where each carbon is covered in hydrogen; One end of the chain has a carboxyl group (-COOH)
Vary in length and #/location(s) of double bonds
Glycerol is a 3-carbon alcohol with a hydroxyl group attached to each carbon
Fats separate from water because water forms hydrogen bonds with itself while excluding the fats
In order to be made, each of the carboxyl groups of the 3 fatty acids must react with one of the 3 hydroxyl groups of the glycerol molecule via dehydration synthesis
bond=ester linkage
Saturated fatty acid
No double bond
Carbon chain completely filled (“saturated”) with hydrogen
Usually solid at room temp.
Unsaturated fatty acid
Double bond along carbon chain, causing a bend
Bend allows triglyceride to become LESS dense, making it liquid at room temperature
Polyunsaturated fatty acid has multiple double bonds within the fatty acid, causing many bends
Phospholipids
2 fatty acid “tails” + 1 negatively charged phosphate “head”
Tails are hydrophobic, while head is hydrophilic (negative charge on head attracts polar water)
Amphipathic molecule (molecule that is both polar and nonpolar)
In water, phospholipids self-assemble into a “bilayer arrangement”
Hydrophobic tails face towards interior
Found in cell membranes
Steroids
Cholesterol
4-ringed molecule dispersed throughout membrane
Maintains membrane stability
Increases membrane fluidity at lower temperatures by disrupting close packing
Decreases fluidity at high temperatures through its constant movement
Nucleic Acids
Contain carbon, hydrogen, oxygen, nitrogen, and phosphorous
Structure
Nitrogenous base
Pentose sugar
Phosphate group
Portion of nucleotide w/o phosphate group is called nucleoside
Store, transmit, and help expres hereditary information
monomer=nucleotides
Amino acid sequence of a polypeptide is programmed by a unit of inheritance called a gene
Made up of DNA
Deoxyribonucleic acid (DNA)
sugar=deoxyribose
Contains genetic/hereditary information
Provides directions for its own replication
Directs synthesis of messenger RNA (mRNA), and through mRNA, controls protein synthesis
Occurs on ribosomes
Ribonucleic acid (RNA)
sugar=ribose
Essential for protein synthesis
2 families of nitrogenous bases
Pyrimidines
Single 6-membered ring
Ex.
Cytosine
Thymine (only DNA
Uracil (only RNA)
Purines
6-membered ring fused to a 5-membered ring
Ex.
Adenine
Guanine
Nucleotide Polymers
Nucleotide polymers linked together to build a polynucleotide
Adjacent nucleotides are joined by covalent bonds that form between the -OH group on the 3’ carbon of one nucleotide and the phosphate on the 5’ carbon on the next
Links create a backbone of sugar-phosphate units with nitrogenous bases as appendages
RNA molecules usually exist as single polypeptide chains
DNA molecules have 2 polynucleotides spiraling around an imaginary axis, forming a double helix
Two backbones run in opposite 5’→3’ directions from each other (antiparallel)
One DNA molecule contains many genes
Nitrogenous bases pair up and form hydrogen bonds
Adenine-Thymine
Guanine-Cytosine
Complementary base pairing
In RNA, thymine is replaced by uracil, so A and U pair
Macromolecule | Monomer | Polymer | Linkage Bond |
Carbohydrates | Monosaccharide (ex. Glucose) | Polysaccharide (ex. Starch, glycogen, cellulose) | Glycosidic linkage |
Proteins | Amino Acid (Ex. Glycine) | Polypeptide (ex. actin) | Peptide bond |
Nucleic Acids | Nucleotides (ex. Adenine, thymine, guanine, cytosine) | DNA or RNA | Sugar-phosphate phosphodiester bonds |
Lipids | Not a true polymer, but often contains chains of carbons with hydrogens | Triglycerides, Phospholipids, cholesterol | Ester bonds |
F. Origins of the Earth
Alexander Oparin and J. B. S. Haldane proposed that the primitive atmosphere contained the following gases:
Methane (CH4)
Ammonia (NH3)
Hydrogen (H2)
Water (H2O)
No free oxygen (O2)
No oxidation/reduction
Rocks do not release oxygen through weathering
Gases collided, producing chemical reactions that eventually led to the organic molecules we know today
Substantial support until 1953
1953, Stanley Miller and Harold Urey simulated the conditions of primitive Earth in a lab,
Put theoried gases into flask, struck them with electrical charges to simulate lightning, and organic compounds similar to amino acids appeared
Current theory of the origin of life suggests 4 main stages
1. Formation of amino acids
2. Monomers form polymers
3. Enclosure of small organic molecules into larger ones
4. Self-replicating molecules that can direct synthesis of other organic substances
Energy sources for early organic synthesis
Lightning
Volcanic eruptions
RNA world hypothesis
Original life-forms were simple molecules of RNA
RNA not restricted to double helix
RNA capable of replicating and passing genes
Complex organic compounds must have formed via dehydration synthesis
Organic compounds then used as food by cells
Simple cells evolved into complex cells