Chapter 10 Structure and nomenclature of organic compounds Flashcards

1
Q

Achiral

A

Not chiral

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2
Q

Alkyl group

A

A group obtained by removing a hydrogen atom from an alkane, with a general formula CnH2n+1. For example, methyl is -CH3. Alkyl groups make up branches in organic compounds.

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3
Q

Chin isomers

A

An isomer of an organic molecule cause by branching of the hydrocarbon chain

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4
Q

Chiral

A

A chiral object is non-superimposable on its mirror image. A chiral molecule has two optical isomers called enantiomers. Chiral molecules do not have a plane of symmetry

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5
Q

Chiral centre

A

A carbon atom which is attached to four different groups in a tetrahedral arrangement.

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6
Q

Cis isomers

A

An isomer in which the highest priority groups attached to the carbons of a double bond are on the same side of the double bond plane

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7
Q

Cis-trans isomers

A

Isomers that occur when two different groups are attached to each carbon in a carbon-carbon double bond. They occur because there is restricted rotation around the carbon-carbon double bond

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8
Q

Enantiomers

A

One of a pair of molecules which are mirror images of each other but which cannot be superimposed. Enantiomers are optical isomers

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9
Q

Functional group

A

An atom or group of atoms in an organic molecule which largely determines the molecule’s properties and reactions

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10
Q

Geometric isomers

A

A type of stereoisomer which can arise when there is restricted rotation in a molecule such as occurs around a carbon-to-carbon double bond or in a ring structure.

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11
Q

Homologous series

A

A series of organic compounds in which each member of the group differs from the previous member by -CH2. Examples are alkanes, alkenes and alcohols

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12
Q

Hydrocarbon

A

A compound which contains only hydrogen and carbon atoms. Examples are alkanes and alkenes

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13
Q

Isomers

A

Molecules which have the same molecular formula but which have different arrangements of atoms in 3-D space.

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14
Q

Molecular formula

A

A formula which gives the type and number of atoms in a molecule.

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15
Q

Optical isomers

A

A type of stereoisomer which can arise when there is restricted rotation in a molecule such as occurs around a carbon-to-carbon double bond or in a ring structure.

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16
Q

Organic molecule

A

A molecule based on a hydrocarbon skeleton. Organic molecules also commonly contain other non-metal elements, such as oxygen, nitrogen, sulphur and chlorine.

17
Q

Postitional isomers

A

Isomers which arise because of different positions of the functional groups on the carbon chain

18
Q

Primary alcohol

A

An alcohol in which the carbon that is bonded to the -OH group is attached to only one alkyl group

19
Q

Saturated

A

Describes hydrocarbons or organic molecules with only single carbon-to-carbon bonds

20
Q

Secondary alcohol

A

An alcohol in which the carbon that is bonded to the -OH group is also attached to two alkyl groups. The alkyl groups may be the same or different

21
Q

Semi-structural formula

A

A formula which summarises the structure of a molecule in a single line of text

22
Q

Skeletal formula

A

A formula which represents the structural arrangement of atoms in a molecule where covalent bonds are represented as lines and where the symbols for carbon and hydrogen are omitted and where C-H bonds are not shown.

23
Q

Stereoisomers

A

Comprise optical isomers and geometric isomers. Stereoisomers are isomers where all the atoms are connected in the same order, but which still have different arrangements in 3-D space.

24
Q

Structural formula

A

A formula which represents the three-dimensional arrangement of atoms in a molecule

25
Structural isomers
Comprise chain isomers and positional isomers, where the molecular formulae are the same but where the atoms are arranged in different ways, structurally.
26
Tertiary
An alcohol in which the carbon that is bonded to the -OH group is also attached to three alkyl groups. The alkyl groups may be the same or different
27
Tetrahedral
In the shape of a tetrahedron, where four points at equal distances are spread as far apart as possible in three dimensions.
28
Trans isomers
An isomer in which the highest priority groups attached to the carbons of a double bond are on opposite sides of the double bond plane.
29
Unsaturated
Describes hydrocarbons or organic molecules containing one or more double or triple carbon-to-carbon bonds