Module 4 - chapter 11 key terms Flashcards

1
Q

Hydrocarbon

A

An organic compound consisting of hydrogen and carbon atoms only

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2
Q

Saturated hydrocarbon

A

Hydrocarbons that have only single bonds between adjacent carbon atoms

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3
Q

Unsaturated hydrocarbons

A

Hydrocarbons that have double or triple covalent bonds between adjacent carbon atoms

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4
Q

Aliphatic hydrocarbon

A

A compound containing carbon and hydrogen joined together in straight chains, branched chains or non-aromatic rings

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5
Q

Alicyclic hydrocarbon

A

An aliphatic compound arranged in non-aromatic rings with or without side chains

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6
Q

Functional group

A

The group of atoms responsible for the characteristic reactions of a particular compound

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7
Q

Homologous series

A

A series of organic compounds having the same functional group, but with each successive member differing by CH2, they have the same general formula.

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8
Q

Structural Isomers

A

Structural isomers are compounds with the same molecular formula but a different structural formula

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9
Q

Stereoisomers

A

organic molecules with the same molecular formula and structural formula but having different arrangements of atoms in space.

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10
Q

Cahn ingold prolog rules

A

1) locate the double bond
2) On each carbon, look at the two substituents. Assign a priority to each group attached to the carbon based on its relative atomic mass. The highest priority group is the one with the highest relative atomic mass.
3) do the same with the other carbon, if the two highest priority groups are on the same side it is a Z isomer, if not its E.

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11
Q

How to tell if somethings a Z isomer?

A

If the two groups with the highest priority are on the same side of the double bond.

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12
Q

How to tell if something is an E isomer?

A

If the two groups with the highest priority are on different sides of the double bond.

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13
Q

What are cis-trans isomers?

A

are pairs of molecules which have the same formula but whose functional groups are rotated into a different orientation in three-dimensional space. For example the atoms coming off the top of the double bond being the same and the atoms coming off the bottom of the double bond being the same.

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14
Q

Covalent bond

A

The electrostatic attraction between a shared pair of electrons and the nuclei of the bonded atoms.

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15
Q

Homolytic fission

A

The breaking of a covalent bond, with one of the bonded electrons going to each atom. Two radicals form.

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16
Q

Heterolytic fission

A

the breaking of a covalent bond with BOTH of the bonded electrons going to ONE of the atoms forming a Cation (+) and an anion (-).

17
Q

A radical

A

a species with an unpaired electron (they’re very reactive)

18
Q

Aromatic

A

Some or all of the carbon atoms are joined together in a benzene ring.

19
Q

Alkynes

A

Containing at least one triple carbon-carbon bond

20
Q

Molecular formulae

A

The molecular formula shows the number and type of atoms of each element present in a molecule.

21
Q

Empirical formula

A

The simplest whole-number ratio of atoms of each element present in a molecule.

22
Q

General formula

A

Is the simplest algebraic formula for any member of a homologous series.

23
Q

Displayed formula

A

Shows the relative positioning of all the atoms in a molecule and all the bonds between them.

24
Q

Structural formula

A

Uses the smallest amount of detail necessary to show the arrangement of atoms in a molecule. Shows which groups are bonded together.

25
Q

Skeletal formula

A

simplified organic formula

26
Q

Addition reaction

A

Two reactants join together to form one product

27
Q

Substitution

A

An atom or group of atoms is replaced by a different atom or group of atoms.

28
Q

Elimination

A

involves the removal of a small molecule from a larger one. One reactant molecule forms two products.