Organic Chemistry Terms Flashcards

Learn and memorize the terms used in chapter 10 of Chemistry SL

1
Q

Saturated

A

Compounds which contain only single bonds (Ex. Alkanes)

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
2
Q

Unsaturated

A

Compounds which contain double or triple bonds (Ex. Alkenes, arenes)

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
3
Q

Aliphatic

A

Compounds which do not contain a benzene ring: may be saturated or unsaturated

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
4
Q

Arenes

A

Compounds which contain a benzene ring: they are all unsaturated compounds (Ex. Benzene, phenol)

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
5
Q

Electrophile (electron-seeking)

A

An electron-deficient species which is therefore attracted to parts of molecules which are electron rich

Electrpphiles are positive ions or have partial positive charge

(Ex. NO2+, H+, Br)

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
6
Q

Nucleophile (nucleus-seeking)

A

An electron-rich species which is therefore attracted to parts oof molecules which are electron deficient

Nucleophiles have a lone pair of electrons and may also have a negative charge

(Ex. Cl-, OH-, NH3)

*Diagram in textbook pg 306

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
7
Q

Addition reaction

A

occurs when two reactants combine to form a sing;e product

Characteristic of unsaturated compounds

Ex. C2H4 + Br2 = C2H4Br2

*Diagram and proper notation in the textbook on page 306

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
8
Q

Substitution Reaction

A

Occurs when one atom or group of atoms in a compound is replaced by a different atom or group

Characteristic of saturated compounds and aromatic compounds

Ex. CH4 + Cl2 = CH3Cl + HCL

*Proper notation on pg 306

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
9
Q

Addition-elimination reaction (Condensation reaction)

A

Occurs when two reactants join together (addition) and in the process a small molecule such as H2O, HCl, or NH3 is lost (elimintation)

Reactants occurs between a functional group in each reactant

Ex. ROH + R’COOH = R’COOH +H2O

*Proper notation and a diagram in the text book on pg 307

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
10
Q

Homolytic Fission

A

Is when a covalent bond breaks by splitting the shared pair of electrons between the two products

Produces two free radicals, each with an unpaired electron

*Diagram on pg 307

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
11
Q

Heterolytic Fission

A

Is when a covalent bond breaks with both the shared electrons going to one of the products

Produces two oppositely charged ions

*Diagram on pg 307

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
12
Q

Homologous Series

A

The members of a homologous series are apart of the same family. The members of a homologous series share common features

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
13
Q

Alkanes

A

Differing by CH2 groups.

Methane, Ethane, Propane, Butane

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
14
Q

Empirical Formula

A

Simplest whole number ratio of the atoms in contains

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
15
Q

Molecular formula

A

The compound is the actual number of atoms of each element present in the molecule

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
16
Q

Structural Formula

A

Representation of the molecule showing how the atoms are bonded to each other

17
Q

Full structual formula

A

Show every atom and bond, angles

18
Q

Condensed structural formula

A

Often omits bonds where they can be assumed, and groups atoms together. Contains the minimum information needed to describe the atom non-ambiguously

19
Q

Stereochemical formula

A

attemps to show the realtive positions of atoms and groups around in three dimensions. The convention is that a bond sticking forwards from the page is shown as a solid, enlarging wedge, whereas a bond sticking behind the page is shown as a hashed line…

*More is the textbook on pg 312
*Diagram/table in text on pg 312

20
Q

What is the first step in naming am organic compound using the IUPAC system?

A

Identifying the longest straight chain of carbon atoms. This gives the tem of the name, (Ex. Meth-, Eth-, Prop-, But-, Pent-, Hex-…)

21
Q

What is the second step in naming am organic compound using the IUPAC system?

A

Identify the functional group

22
Q

Functional Group

A

a specific group of atoms or bonds within a compound that is responsible for the characteristic chemical reactions of that compound

23
Q

What does the number infront or in the middle of a name indicate?

A

Which carbon the functional group is attached to

24
Q

What is the third step in naming am organic compound using the IUPAC system?

A

Identify the side chains

25
Q

What is the name for an alkane side group?

A

Methyl, ethyl, propyl, etc

26
Q

What is a halogenoalkane?

A

Fluoro, chloro, bromo, iodo

27
Q

What is the prefix for an amine being used as a subsituent?

A

Amino-

28
Q

Structural isomers

A

Different arrangement of same atoms

(ex. C4H10 can be drawn as butane and 2-methylpropane)

29
Q
A