Introduction to Organic Chemistry Flashcards

Be familiar with the topic.

1
Q

Definition of Aliphatic Hydrocarbon

A

Open chains of Carbon atoms

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2
Q

Definition of Alicyclic Hydrocarbon

A

Closed rings of Carbon atoms

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3
Q

Definition of Aromatic Hydrocarbon

A

Hydrocarbon containing a benzene ring

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4
Q

Functional group

A

A group within an organic compound responsible for its characteristic chemical properties

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5
Q

Homologous Series

A

A family of compounds containing the same functional group

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6
Q

Empirical formula

A

Shows the simplest ratio of different type of atoms in a molecule

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7
Q

Molecular formula

A

Shows the actual number of each type of atom in a molecule

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8
Q

Condensed structural formula

A

Shows how groups of atoms are arranged sequentially

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9
Q

Displayed/Full structural formula

A

Shows all bonding in a molecule

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10
Q

Stereochemical structure

A

Shows spatial structure of a molecule

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11
Q

Skeletal formula

A

Shows the carbon skeleton with any functional group

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12
Q

Homolytic Fission

A

The breaking of a covalent bond such that one electron goes to each of the atom, forming of free radicals

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13
Q

Heterolytic Fission

A

The breaking of a covalent bond such that the bonding electrons goes to the same atom, forming positive and negative ions.

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14
Q

Degree of substitution

A

Determined by the number of alkyl or aryl groups bonded to it

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15
Q

Electrophile

A

Electron pair acceptor: Electron deficient species and are attracted to regions of negative charge/electron rich sites

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16
Q

Nucleophile

A

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

17
Q

Free radical

A

Electrically neutral and contains an unpaired electron formed from homolytic fission

18
Q

Electronic effect

A

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

19
Q

Steric hindrance

A

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

20
Q

Isomerism

A

Existence of two or more compounds with the same molecular formula but different arrangement of atoms.

21
Q

Constitutional/Structural Isomerism

A

Molecules with the same molecular formula but different structural formula

22
Q

Stereoisomerism

A

Existence of two or more compounds with the same molecular formula and structural formula but different spatial (3D) arrangement of atoms

23
Q

Cis-Trans Isomerism

A

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.

24
Q

Enantiomers

A

Compounds with the same molecular and structural formula but with different spatial arrangement of atoms

  1. It form an non-superimposable mirror image
  2. It does not have a plane of symmetry
  3. It contains one or more chiral centers
25
Q

Chiral carbon

A

It is a SP3 hybridised carbon atom and has four different groups attached to it.

26
Q

Meso compound

A

Molecules which are superimposable on their mirror images. Contains a plane of symmetry.