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
Q

Structural isomers

A

Comprise chain isomers and positional isomers, where the molecular formulae are the same but where the atoms are arranged in different ways, structurally.

26
Q

Tertiary

A

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
Q

Tetrahedral

A

In the shape of a tetrahedron, where four points at equal distances are spread as far apart as possible in three dimensions.

28
Q

Trans isomers

A

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
Q

Unsaturated

A

Describes hydrocarbons or organic molecules containing one or more double or triple carbon-to-carbon bonds