Introduction to Organic Chemistry Flashcards
Be familiar with the topic.
Definition of Aliphatic Hydrocarbon
Open chains of Carbon atoms
Definition of Alicyclic Hydrocarbon
Closed rings of Carbon atoms
Definition of Aromatic Hydrocarbon
Hydrocarbon containing a benzene ring
Functional group
A group within an organic compound responsible for its characteristic chemical properties
Homologous Series
A family of compounds containing the same functional group
Empirical formula
Shows the simplest ratio of different type of atoms in a molecule
Molecular formula
Shows the actual number of each type of atom in a molecule
Condensed structural formula
Shows how groups of atoms are arranged sequentially
Displayed/Full structural formula
Shows all bonding in a molecule
Stereochemical structure
Shows spatial structure of a molecule
Skeletal formula
Shows the carbon skeleton with any functional group
Homolytic Fission
The breaking of a covalent bond such that one electron goes to each of the atom, forming of free radicals
Heterolytic Fission
The breaking of a covalent bond such that the bonding electrons goes to the same atom, forming positive and negative ions.
Degree of substitution
Determined by the number of alkyl or aryl groups bonded to it
Electrophile
Electron pair acceptor: Electron deficient species and are attracted to regions of negative charge/electron rich sites
Nucleophile
Electron pair donor: Electron rich species, which possess at least one lone pair of electrons and are attracted to regions of positive charge/electron deficient sites
Free radical
Electrically neutral and contains an unpaired electron formed from homolytic fission
Electronic effect
Due to donation/withdrawal of electron through sigma bonds due to the electronegativity difference between atoms.
Delocalization of lone pair of electron into the pi electron cloud of benzene OR Delocalization of pi electron cloud onto the substituent
Steric hindrance
Occurs when a substituent hinders an approach of an attacking reactant and either prevents a reaction/lowers reactivity of a particular site of the molecule
Isomerism
Existence of two or more compounds with the same molecular formula but different arrangement of atoms.
Constitutional/Structural Isomerism
Molecules with the same molecular formula but different structural formula
Stereoisomerism
Existence of two or more compounds with the same molecular formula and structural formula but different spatial (3D) arrangement of atoms
Cis-Trans Isomerism
In order to exist:
1. Restricted rotation about a double bond/ a ring structure
2. For an alkene, each carbon atom in double bond must have two different groups attached to it.
3. For a cyclic compound, two or more of the carbon atoms in the ring have two different groups attached.
Enantiomers
Compounds with the same molecular and structural formula but with different spatial arrangement of atoms
- It form an non-superimposable mirror image
- It does not have a plane of symmetry
- It contains one or more chiral centers
Chiral carbon
It is a SP3 hybridised carbon atom and has four different groups attached to it.
Meso compound
Molecules which are superimposable on their mirror images. Contains a plane of symmetry.