Biochemistry Flashcards
Unique properties of Carbon
1) Tends to four form covalent bonds
2) Often forms double and triple bonds, particularly with othe carbon atoms
3) Catenates more often than any other atoms
Organic molecule
Molecules containing Carbon
Catenate
Verb used to describe the action of atomically bonded chains
Organic chemistry
The study of how carbon-containing molecules interact with other carbon-containing molecules
Alkanes
Single bond hydrocarbon molecules
Alkenes
Double bond hydrocarbon molecules
Alkynes
Triple bond hydrocarbon molecules
Hydrocarbons
Compounds that contain both carbon and hydrogen
Structural formula
Formulas that show not only the number of atoms but the manner in which the atoms are arranged and bonded together
Structural isomers
Molecules of the same chemical formula, but different arrangements
Types of hydrocarbons
1) Aromatic hydrocarbons
2) aliphatic hydrocarbons (include alkanes, alkenes, alkynes)
Stereoisomers
Molecules with the same conectivity but different spacial arrangements
Connectivity
The types of bonds that hold the atoms together
Spatial arrangement
The manner in which atoms are arranged in relation to one another
Optical isomers
Type of stereisomer that is a mirror image of the natural molecule
(Also called enantiomers)
Enantiomers
Type of stereisomer that is a mirror image of the natural molecule
(Also called optical isomers)
Geometric isomers
A form of stereoisomers involving the orientation of functional groups in a molecule that contains bonds of incompatible rotating
Chiral
The either molecule in a mirror isomer situation
Dextrorotatory isomers
An optical isomer that rotates the polarization of light clockwise
Levorotory isomer
An optical isomer that rotates the polarization of light counter-clockwise
Racemic mixture
A mixture of both levorotatory and dextrorotary isomers that cancel each other out so that the polarized light is not rotated at all
Saturated hydrocarbons
When a carbon or chain of carbons is bonded to as many hydrogens as it can be
Unsaturated hydrocarbon
A hydrocarbon to which hydrogens could still bond
Reaction of alkanes
Undergo substitution reactions in which one or more hydrogen atom is replaced by an atom or group of atoms
Reactions with alkenes and alkynes
Always synthesis reaction, always breaks apart double or triple bonds or a single bond (the bond type of lowest potential energy)
Always visualize by drawing out the molecular geometry
Polar reagents added to unsymetrical alkenes
The positive end (least electronegative) of the reagent adds to the carbon atom that has the most hydrogen atoms
Aromatic hydrocarbons
Forms a ‘nut shaped’ hexagon of centrally bonded carbon atoms
With 3 double bonds and 3 single bonds
See book for specific notation
Benzenes
An aromatic hydrocarbon in which only one carbon atom has been substituted.
Takes the form (substituent name)benzene
Phenal group
The name of the long string of hydrocarbons used as the substituent in the carbon hexagon
Di-substituted benzenes
Benzezne in which two hydrocarbons have been substituted
Reactions of aromatic compounds
Given as the reaction between a benzene molecule and another compound
Polycyclic aromatic compounds
Aromatic compounds in which individual rings are fused together
Functional group
A characteristic atom or group of atoms that give the molecule certain qualities
Alcohols
molecules containing a hydroxal group (OH-)
Bonded to the lowest carbon atom
End in ‘-ol’ suffix
Meth- prefix
1 hydrocarbon
Eth- prefix
2 hydrocarbons
Prop- prefix
Three hydrocarbons
But- prefix
Four hydrocarbons
Pent- prefix
Five hydrocarbons
Hex- prefix
Six hydrocarbons
Hept- prefix
Seven hydrocarbons
Oct- prefix
Eight hydrocarbons
Non- prefix
Nine hydrocarbons
Dec- prefix
Ten hydrocarbons