Unit 1 test review two

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Created by:

itsreelygreat5  on September 19, 2010

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ap bio ii

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Unit 1 test review two

temperature
average kinetic energy of molecules
1/80
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Terms

Definitions

temperature average kinetic energy of molecules
heat of vaporization the quality of heat a liquid must absorb for 1 gram of it to be converted from liquid to gas
evaporative cooling occurs because the hottest molecules (greatest kinetic energy) are the most likely to leave as gas; contributes to stability of temperature
specific heat the amount of heat that must be absorbed or lost for 1 gram of that substance to change its temperature by 1 degree Celsius
hydrophilic substances substances attracted to water, whether ionic or polar
colloids components suspended in the aqueous liquid of the cell because they are such large molecules they don't dissolve
hydrophobic substances substances that are not attracted to, or do not have an affinity for water; nonionic and nonpolar substances
solution a mixture that is completely homogeneous
solvent the dissolving agent
solute the substance that is dissolved
aqueous solution solution where water is the solvent
hydration shell the sphere of water moleculres around each dissolved ion
molecular mass the sum of the masses of all the atoms in a molecule
mole 6.02 x 10^23 daltons in 1 gram; Avogadro's number
molar mass the mass of 6.02 x 10^23 molecules of a substance
molarity the number of moles of solute per liter of solution
hydronium ion when a water molecule breaks down into a hydrogen ion and a hydroxide ion, the lone hydrogen ion connects to another water molecule to form this
hydroxide OH-
hydronium H30+
acid a substance that increases the hydronium ion concentration
base a substance that reduces the hydronium concentration
buffers substances that minimize changes in concentrations of H+ and OH- in a solution; usually acid/base pairs
vitalism outside force put organic matter here; belief in supernatural force creating organic matter
mechanism belief that organic matter can be created according to laws of physics and chemistry
Wohler makes urea in lab 1828
Kolbe acetic acide made in lab synthetically
Miller 1953 simulated early earth conditions to make organic compounds
hydrocarbons molecules of hydrogen and carbon only; main componenets of fossil fuels; can be diverse in length and shape; hydrophobic; often nonpolar
"ane" ending for hydrocarbon with all single bonds
"ene" ending for hydrocarbon with double bond
"yne" ending for hydrocarbon with triple bond
isomer same molecular formula, different structure/properties
structural isomers rearranging the carbon backbone
geometric isomers same covalent partnership, different spatial arrangements (surrounding double bonds)
enantiomers asymmetric carbons, mirror-image molecules, left-hand/right-hand molecules
functional groups certain groups of atoms that frequently attach to the carbon chain
hydroxyl -OH; tend to form alcohols; tend to change to a polar molecule (hydrophilic)
carbonyl =O; double-bonded oxygen on middle carbons - ketones; double-bonded oxygen on end carbons - aldehydes
carboxyl -C-OH and =O; form carboxylic acids; can become ionized (release H+) makes it acidic
amino group -N-H and -H; form amines; can become ionized by accepting an H+, tend to be basic
sulfhydryl -SH; form thiols; help stabilize proteins
phosphate group -O-P-O_ and =O and -O_; form organic phosphates; associated with energy transfers (ATP/ADP)
monomer subunit or building block molecule
polymer large molecule consisting of many similar subunits connected together
macromolecule large organic polymer
condensation reaction monomers are covalently linked, producing net removal of water molecule for each linkage; one monomer loses OH- and the other monomer loses a hydrogen
hydrolysis breaking polymers into monomers
carbohydrates made of monomers called monosaccharides (mol. form. mult. of CH2O); hydroxyl off each C except for 1 carbonyl; -OSE ending; sugars form rings
glycosidic linkage monosaccharides link in condensation reaction called this
disaccharides maltose (2 glucoses); lactose (glucose + galactose); sucrose (glucose + frucose)
starch consists entirely of glucose molecules; joined by 1-4 linkages, helical shape; in A configuration
amylose unbranched starch
amylopectin branched starch with 1-6 linkages at branch points
glycogen polymer of glucose more extensively branched than amylopectin
cellulose major componenet of plant cell walls; most abundant organic compound; polymer of glucose, but in B configuration; never branched/straight
chitin used by arthropodes tto build exoskeletons; similar to cellolose, except glucose monomer of this has nitrogen-containing appendage
fats large molecules not polymers; made of glycerol and a fatty acid
glycerol an alcohol with 3 carbons each with hydroxyl
fatty acid long carbon skeleton 16-18 carbons with carboxyl group
saturated fat all single bond fatty acid tail; tend to be solids at room temp
unsaturated fat one or more double bonds; oils tend to be liquids at room temp
hydrogenated makes unsaturated, saturated
ester linkage condensation reaction that links the fatty acid to the glycerol
phospholipids gylcerol with 2 fatty acids and 3rd spot joined with phosphate group; tails hydrophobic and heads hydrophilic; main part of membrances
steroids 4 interconnected carbon rings; differ by functional groups attached to rings
proteins monomers are amino acids; make up large part of organisms
polypeptide chain of amino acids; need arranging before protein level
peptide bond condensation reaction bonding amino acids together
primary structure protein's unique sequence of amino acids; order
secondary structure consists of coils or folds of polypeptide chains that contribute to the protein's overall conformation, the result of hydrogen bonds between the repeating constituents of the polypeptide backbone
tertiary structure the overall shape of a polypeptide resulting from interactions between the R groups of the various amino acids
quaternary structure the overall protein structure that results from the aggregation of those polypeptide subunits; several chains
denaturation if environment is altered, protein may unravel and lose its native conformation
nucleotides monomers of nucleic acids; 3 parts include pentose sugar (ribose or deoxyribose), phosphate group, nitrogenous base
pyrimidines single ring structure of nitrogenous base; cytosine, thymine, uracil (takes place of thymine in RNA)
purines double ring structure of nitrogenous base; adenine and guanine
phosphodiester linkage nucleotides linked together by this; connects the 3' carbon of one nucleotide to the phosphate group of another nucleotide
pairs of nitrogenous bases A and T connected by 2 hydrogen bonds; G and C connected by 3 hydrogen bonds
RNA single chain of nucleotides; has ribose sugar; has U, C, A, G
DNA forms double helix; provides direction for its own replication; provides coded info to make RNA

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