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Biochem Midterm Defintions
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Ability of carbon to form bonds with other elements or itself, including single, double, and triple bonds.
Bonding properties of carbon (Clue: Main reason organic chemistry has so many compounds)
Number of covalent bonds an atom can form.
Covalency number (Clue: For carbon it’s 4, for oxygen it’s 2, etc.)
Covalency number of carbon.
4 (Clue: Tetravalent — can bond to four other atoms)
Covalency number of oxygen.
2 (Clue: Think of water — oxygen bonds to two hydrogens)
Covalency number of hydrogen.
1 (Clue: Only needs one bond to be stable)
Covalency number of bromine.
7 valence electrons / covalency often 1 (Clue: Halogen group — one bond to be stable)
Covalency number of nitrogen.
3 (Clue: Think ammonia — nitrogen bonds to three hydrogens)
Type of bond formed between carbon and hydrogen.
Carbon–Hydrogen bond (Clue: Found in almost every organic compound)
Type of bond formed between carbon and halogens like Cl, Br, I.
Carbon–Halogen bond (Clue: Found in alkyl halides)
Bond between two carbon atoms that may be single, double, or triple.
Carbon–Carbon bond (Clue: Basis of carbon chains and rings)
Combination of carbon bonded to hydrogen and halogen atoms.
Carbon–Hydrogen–Halogen bond combination (Clue: Example: CH₃Br)
Formula that shows the actual number of each type of atom in a molecule.
Molecular formula (Clue: Example: C₂H₆)
Formula that shows how atoms are connected in a molecule.
Structural formula (Clue: Every bond is drawn out)
Formula that shows atoms in a simplified arrangement without showing every bond.
Condensed structural formula (Clue: Example: CH₃CH₂CH₃ for propane)
Formula that uses lines to represent bonds and omits carbon/hydrogen symbols.
Skeletal/line formula (Clue: Zig-zag lines where each corner is a carbon)
Compounds with the same molecular formula but different structures.
Isomers (Clue: Same “ingredients,” different arrangement)
Example of structural isomers where arrangement of carbon atoms differs.
Butane and isobutane (Clue: Both are C₄H₁₀)
Example of isomers where the location of the double bond differs.
Double bond position isomers (Clue: Example: 1-butene vs 2-butene)
Compounds with identical structure and bonding, not isomers.
Same compounds (Clue: Same molecular and structural formula)