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Chemistry A22
Definitions
Term | Definition |
---|---|
base peak | Peak of greatest abundance in a mass spectrum. |
molecular ion peak | A peak produced by an ion formed by the removal of one electron from a molecule. |
M+1 peak | A peak produced by a molecular ion with an increased mass due to the presence of one carbon-13 atom. |
Fragmentation ion | A positively charged ion produced when the molecular ion breaks apart. |
Low resolution nmr | A spectrum which does not show the spin-spin splitting pattern. |
High resolution nmr | A spectrum which does show the spin-spin splitting pattern. |
Doublet | A signal which appears as a pair of lines of equal intensity ` |
triplet | A signal which appears as three lines in the approximate intensity ratio (1:2:1) |
quartet | A signal which appears as four lines in the approximate intensity ratio (1:3:3:1) |
back titration | Method where an excess of a reagent is reacted with a sample. The unreacted reagent is then determined by titration. |
Rf value | Retardation factor, this is calculated using the expression: Rf =Distance moved by spot/Distance moved by solvent |
Retention time | The time taken from injection until a component reaches the detector. |
Transition metal | An element which forms at least one stable ion with a partially filled d-subshell |
Complex | A central metal atom or ion with ligands bonded by co-ordinate bonds. |
ligand | An ion or molecule with a lone pair of electrons which forms a co-ordinate bond with a central metal atom or ion in a complex. |
Co-ordination number | The number of co-ordinate bonds to a central metal atom or ion in a complex. |
Monodentate | A ligand which uses only one lone pair of electrons to form a co-ordinate bond with a central metal atom or ion in a complex. |
Bidentate | A ligand which uses two lone pairs of electrons to form two co-ordinate bonds with a central metal atom or ion in a complex |
Polydentate | A ligand which uses many lone pairs of electrons to form more than two co-ordinate bonds with a central metal atom or ion in a complex. |
Standard electrode potential | the potential difference measured when a half-cell is connected to the standard hydrogen electrode under standard conditions. |
emf | The potential difference measured when two half-cells are connected. |
Primary amine | Only one carbon atom directly bonded to the nitrogen atom and therefore has the (-NH2) group. |
Secondary amine | Two carbon atoms directly bonded to the nitrogen atom i.e. NH |
Tertiary amine | Three carbon atoms directly bonded to the nitrogen atom i.e. N |
Coupling | A reaction in which two benzene rings are linked together through an azo (-N=N-) group. |
Dehydration of amides | A reaction which involves the elimination of water from the amide. |
Zwitterions | Ions which have a permanent positive and negative charge but which are neutral overall. |
Primary structure (protein) | Sequence of amino acids joined by peptide links in the chain. |
Secondary structure (protein) | The twisting/coiling of the chain to form a β-pleated sheet/α helix by intramolecular hydrogen bonding |
Tertiary structure (protein) | The bending/folding of the secondary structure to give a precise 3D shape held together by hydrogen bonding/disulfide bridges/ionic interactions/van der Waals’ forces. |
Enzyme | A protein which is a biological catalyst. |
Active site | The site on the surface of the enzyme into which the substrate fits. |
Induced fit | The substrate induces a change of shape of the active site of the enzyme |
Condensation polymers | Polymers formed by the elimination of small molecules such as water or hydrogen chloride when monomers bond together. |
Biodegradable polymer | A polymer which can be hydrolysed by the action of microorganisms. |
DNA replication | The process by which a double stranded DNA molecule is copied to produce two identical DNA molecules. |
GLC-MS | A gas liquid chromatograph attached to a mass spectrometer. |
Sequestering | The formation of a complex so that an ion is no longer available for reactions. |