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This set of flashcards covers vocabulary and key concepts from Chapter 3 and 4 regarding water's properties, pH, and the structural diversity of carbon-based organic molecules.
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Polar molecule
A molecule, such as water, where the overall charge is unevenly distributed.
Partial negative charge (8â)
The charge at the oxygen end of a water molecule because oxygen pulls electrons toward itself.
Partial positive charge (8+)
The charge at the hydrogen atoms' end of a water molecule.
Hydrogen bonds
Weak attractions between oppositely charged regions of water molecules that allow them to bond to each other.
Cohesion
The attraction between like molecules, such as water molecules sticking to each other.
Adhesion
An attraction between different substances, such as between water and plant cell walls.
Surface Tension
A property of water, illustrated by the raft spider, resulting from the cohesiveness of water molecules.
Moderation of Temperature
Water's ability to absorb heat from warmer air and release stored heat to cooler air with only slight changes in its own temperature.
Specific Heat
The amount of heat required for 1calorie of energy to heat a gram of water by one degree.
Specific Heat of Water Value
1calorie/(gâ 0Ë0baC).
Calorie
A unit of heat energy mentioned in the context of warming water.
High Heat Capacity
A result of water resisting temperature changes because it takes a lot of energy to break hydrogen bonds.
Kinetic Energy
The energy of motion.
Thermal Energy
The kinetic energy associated with the random motion of atoms or molecules.
Heat
Thermal energy in transfer from one body of matter to another.
Temperature
A measure representing the average kinetic energy of the molecules in a body of matter.
Absorption of Heat
The process that occurs when hydrogen bonds in water break.
Release of Heat
The process that occurs when hydrogen bonds in water form.
Evaporation (Vaporization)
The transformation of a substance from a liquid state to a gaseous state.
Evaporative Cooling
A process where the remaining surface of a liquid cools as it evaporates, helping to stabilize temperatures.
Crystalline Lattice
The structure water molecules are locked into at 0âC to form ice.
Water Density at 4âC
The temperature at which water reaches its greatest density.
Ice Density
Ice is approximately 10% less dense than liquid water because hydrogen bonds keep molecules farther apart.
Solution
A liquid that is a completely homogeneous mixture of substances.
Solvent
The dissolving agent of a solution.
Solute
The substance that is dissolved in a solution.
Aqueous Solution
A solution in which water is the solvent.
Hydrophilic
A substance that has an affinity for water.
Hydrophobic
A substance that does not have an affinity for water, such as oil.
Hydrogen Ion (H+)
A single proton with a charge of +1 that leaves its electron behind when a hydrogen atom shifts between water molecules.
Hydroxide Ion (OHâ)
The water molecule that lost a proton during dissociation, carrying a negative charge.
Hydronium Ion (H3âO+)
The molecule with an extra proton, often represented simply as H+.
Acid
A substance that increases the H+ concentration of a solution.
Base
A substance that reduces the H+ concentration of a solution.
Strong Acids and Bases
Substances that dissociate completely when placed in water.
Weak Acids and Bases
Substances that reversibly release and accept back hydrogen ions.
Neutral Solution pH
A solution where the [H+] is 10â7, resulting in a pH of 7.
Product of [H+] and [OHâ]
In any aqueous solution at 25âC, this constant value is 10â14.
pH Scale Definition
Defined by the negative logarithm of H+ concentration: pH=âlog[H+].
Acidic Solutions
Solutions that have pH values less than 7.
Basic Solutions
Solutions that have pH values greater than 7.
Biological Fluid pH Range
The typical pH range of most biological fluids, which is between 6 and 8.
Buffer
A substance that minimizes changes in the concentrations of H+ and OHâ in a solution.
Organic Compounds
Carbon-based molecules that form the basis for all biological molecules.
Carbon Versatility
Carbon's ability to form four bonds, allowing it to make an inexhaustible variety of organic molecules.
Miller-Urey Experiment
An experiment demonstrating that organic molecules may have formed on early Earth through natural chemical reactions.
Major Elements of Life
The elements C, H, O, N, S, and P.
Valence of Carbon
Carbon has 4 valence electrons and can form 4 covalent bonds.
Tetrahedral Shape
The molecular shape formed when a carbon atom is bonded to four other atoms.
Carbon Double Bond Plane
When two carbon atoms are joined by a double bond, all atoms joined to those carbons are in the same plane.
Hydrocarbons
Organic molecules consisting only of carbon and hydrogen.
Carbon Skeleton
The chain of carbon atoms that forms the structural backbone of an organic molecule.
Isomers
Compounds with the same molecular formula but different structures and properties.
Structural Isomers
Isomers that have different covalent arrangements of their atoms.
Cis-trans Isomers
Isomers that have the same covalent bonds but differ in their spatial arrangements; also known as geometric isomers.
Enantiomers
Isomers that are mirror images of each other.
cis Isomer
A spatial arrangement where two identical groups (X) are on the same side of a double bond.
trans Isomer
A spatial arrangement where two identical groups (X) are on opposite sides of a double bond.
S-Ibuprofen
The effective enantiomer of ibuprofen used to reduce inflammation and pain.
R-Albuterol
The effective enantiomer of albuterol used to relax bronchial muscles in asthma patients.
Functional Groups
Specific components of organic molecules most commonly involved in chemical reactions.
Hydroxyl Group
The chemical group -OH, found in alcohols like ethanol.
Carbonyl Group
The chemical group C=O, found in ketones and aldehydes.
Carboxyl Group
The chemical group -COOH, found in carboxylic acids or organic acids.
Amino Group
The chemical group -NH2â, found in amines like glycine.
Sulfhydryl Group
The chemical group -SH, also known as a thiol group, found in compounds like cysteine.
Phosphate Group
The chemical group -OPO32ââ, found in organic phosphates like glycerol phosphate.
Methyl Group
The chemical group -CH3â, found in methylated compounds like 5-Methylcytosine.
Alcohol
A compound name for molecules containing a hydroxyl group.
Ketone
A compound where the carbonyl group is within a carbon skeleton, such as acetone.
Aldehyde
A compound where the carbonyl group is at the end of a carbon skeleton, such as propanal.
Carboxylic Acid
A compound containing a carboxyl group, such as acetic acid.
Amine
A compound containing an amino group, such as glycine.
Thiol
A compound containing a sulfhydryl group, such as cysteine.
Organic Phosphate
A compound containing a phosphate group, such as glycerol phosphate.
Methylated Compound
A compound containing a methyl group, such as 5-Methylcytosine.
ATP
Adenosine triphosphate, an important organic phosphate that stores the potential to react with water and release energy.
Adenosine
The organic molecule in ATP that is attached to a string of three phosphate groups.
Triphosphate chain
The group of three phosphate groups found in ATP labeled alpha, beta, and gamma.
Phosphoanhydride bonds
The high-energy bonds linking the phosphate groups in ATP.
Ribose
The 5-carbon sugar component of ATP.
Adenine
The nitrogenous base component of ATP.
Methane (CH4â)
A simple hydrocarbon where carbon forms four bonds with hydrogen in a tetrahedral shape.
Ethane (C2âH6â)
A molecule consisting of two carbons joined by a single bond, with four hydrogens on each end.
Ethene (C2âH4â)
A molecule also known as ethylene where two carbons are joined by a double bond.
Butane
A straight unbranched carbon skeleton with the formula C4âH10â.
2-Methylpropane
A branched carbon skeleton isomer of butane, commonly called isobutane.
1-Butene
A hydrocarbon where the double bond is positioned between the first and second carbons.
2-Butene
A hydrocarbon where the double bond is positioned between the second and third carbons.
Cyclohexane
A common carbon skeleton arranged in a six-carbon ring.
Benzene
A six-carbon ring structure with alternating double bonds.
Steroids
Lipids characterized by a carbon skeleton consisting of four fused rings, such as estradiol and testosterone.
Estradiol
A female sex hormone that is a steroid with specific chemical groups attached to its carbon rings.
Testosterone
A male sex hormone that is a steroid differing from estradiol only in its attached chemical groups.
Dissociation of water
The process where a hydrogen atom shifts between water molecules, forming H+ and OHâ.
Ionized Carboxyl Group
The form of -COOH after it loses a proton (H+), resulting in -COOâ.
Ionized Amino Group
The form of -NH2â after it gains a proton (H+), resulting in -NH3+â.
Electron Configuration
The key to an atom's chemical characteristics and the kinds/number of bonds it will form.
Dopamine
A biological molecule shown in the text that promotes mother-infant bonding.
Propane (C3âH8â)
A three-carbon skeleton unbranched hydrocarbon mentioned as a variation in length.