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CELL BIO CH2

QuestionAnswer
Proton Located in the atomic nucleus, with a mass of 1 g/mol (1 Dalton) and a charge of +1
Neutron Uncharged particle in the atomic nucleus, with a mass of 1 g/mol (1 Dalton)
Electron Orbits the nucleus in electron shells with a -1 charge and negligible mass
Nucleus The dense central core of an atom containing its protons and neutrons
Electron Shell Concentric orbits around the nucleus that accommodate up to 2 (1st shell), 8 (2nd shell), or 18 (3rd shell) electrons
Atomic Number The unique number of protons in an atom's nucleus, defining its element identity
Mass Number / Atomic Weight The sum of protons and neutrons in an atom's nucleus
Chemically Inert vs. Reactive Atoms with full outer shells are unreactive (inert); those with incomplete outer shells are reactive and form chemical bonds
Covalent Bond Strong chemical bond formed when two atoms share pairs of valence electrons
Single vs. Double Covalent Bond Single bonds share 2 electrons (1 pair); double bonds share 4 electrons (2 pairs) and are shorter, stronger, and resist rotation
Nonpolar vs. Polar Covalent Bond Nonpolar bonds share electrons equally; polar bonds share electrons unequally due to differing electronegativities, creating partial charges
Electronegativity An atom's intrinsic ability to pull shared electrons toward itself in a bond
Ionic Bond Noncovalent bond formed by complete electron transfer, producing cations (+) and anions (-) held together in salts
Hydrogen Bond Electrostatic interaction between a partially positive hydrogen atom and an electronegative atom (such as O or N)
Van der Waals Attraction Weak electrostatic force between adjacent atoms caused by transient, random fluctuations in electron clouds
Hydrophobic Interaction Attraction between nonpolar molecules driven by repulsion from surrounding polar water molecules
Bond Strength Ranking Ordered in water as: Covalent > Ionic > Hydrogen > Van der Waals
Hydrophilic vs. Hydrophobic Hydrophilic substances (polar molecules, ions, salts) dissolve in water via hydrogen bonds/electrostatic interactions; hydrophobic substances (nonpolar hydrocarbons) do not dissolve
pH & Buffer pH measures hydrogen ion concentration; buffers cooperate as acid-base systems to maintain stable cellular pH
Mole / Avogadro's Number Standard chemical quantity of 6.022 x 10^(23) particles used to calculate molar solutions
Methyl Group (-CH_3) A nonpolar hydrocarbon functional group
Hydroxyl / Alcohol Group (-OH) A polar functional group containing oxygen and hydrogen
Carbonyl / Ketone Group (=O) A functional group featuring a carbon double-bonded to an oxygen atom
Carboxyl / Carboxylic Acid Group (-COOH) An acidic functional group that dissociates in water to become negatively charged
Ester Group (-COOR) Linkage formed by a condensation reaction between a carboxylic acid and an alcohol
Amine Group (-NH_2) A basic functional group that accepts a proton in water to become positively charged
Amide Group An uncharged polar linkage formed by combining a carboxylic acid and an amine group
Phosphate Group A negatively charged group linked by high-energy phosphoanhydride bonds
Condensation (Dehydration) Reaction Covalently links monomers together while releasing a water molecule
Hydrolysis Reaction Cleaves covalent bonds within polymers by adding a water molecule
Macromolecular Assembly Complex cellular structures (e.g., ribosomes) formed when macromolecules combine via noncovalent interactions
Monosaccharide Single sugar unit with general formula containing hydroxyl groups and an aldehyde (aldose) or ketone (ketose)
Hexose vs. Pentose 6-carbon sugar (e.g., glucose) vs. 5-carbon sugar (e.g., ribose or deoxyribose)
Isomers & a/b links Molecules with identical formulas but different spatial arrangements; alpha and beta ring forms depend on the orientation of the hydroxyl group at C1
Glycosidic Bond Covalent bond connecting sugar units, formed via condensation
Disaccharide, Oligosaccharide, Polysaccharide Carbohydrates made of 2 sugars (disaccharide), 3–10 sugars (oligosaccharide), or >10 to hundreds of sugars (polysaccharide like glycogen, starch, cellulose, chitin)
Amino Acid Protein monomer with a central $\alpha$-carbon bonded to a hydrogen, carboxyl group, amino group, and variable side chain (R group)
Amino Acid Classes Grouped by R group properties into nonpolar, uncharged polar, acidic (negatively charged), or basic (positively charged)
Peptide Bond Rigid, planar covalent amide linkage formed by condensation that connects amino acids in a polypeptide
Conformation & Subunit Conformation is the folded 3D protein structure; a subunit is an individual polypeptide chain within a protein assembly
Nucleotide vs. Nucleoside A nucleotide contains a 5-carbon pentose sugar, a nitrogenous base, and phosphate group(s); a nucleoside lacks phosphate groups
Purines vs. Pyrimidines Purines are double-ring bases (Adenine, Guanine); pyrimidines are single-ring bases (Cytosine, Thymine, Uracil)
Phosphoanhydride Bond High-energy covalent bond linking adjacent phosphate groups in nucleotides like ATP
Phosphodiester Bond Covalent bond linking nucleotides into nucleic acid chains (DNA/RNA) via condensation
DNA vs. RNA DNA is a double-stranded double helix storing genetic information (A, C, G, T; deoxyribose sugar); RNA is a single-stranded transient copy (A, C, G, U; ribose sugar)
Lipid Water-insoluble (hydrophobic) organic molecule used for energy storage and cell membranes
Amphipathic Having both strongly hydrophobic and hydrophilic regions in the same molecule
Fatty Acid Amphipathic lipid with a long hydrophobic hydrocarbon tail and a hydrophilic carboxyl head
Saturated vs. Unsaturated Fatty Acid: Saturated tails have no carbon-carbon double bonds; unsaturated tails contain double bonds that introduce kinks, decreasing packing and increasing membrane fluidity
Triacylglycerol Three fatty acid chains esterified to a glycerol backbone; stored as energy droplets in cells
Phospholipid & Lipid Bilayer Amphipathic lipid (two fatty acids + phosphate + glycerol) that forms self-sealing cell membrane bilayers
Isoprenoids & Sterols Isoprenoids are long-chain polymers of 5-carbon isoprene units (e.g., dolichol phosphate); sterols share a rigid multi-ring hydrocarbon structure (e.g., cholesterol)
Created by: bbrdd
 

 



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