Introduction to Organic Chemistry Flashcards

1
Q

How does Carbon bond?

A
  • Has 4 electrons in its outer shell
  • Can form 4 single bonds
  • Can form 2 double bonds
  • Can form 1 triple bond and 1 single bond
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2
Q

Functional Group

A

Responsible for the different chemical and physical properties of the compound

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3
Q

Homologous Series

A

A group of compounds with the same functional group that differ by a CH2

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4
Q

How can you represent organic compounds?

A
  • Empirical Formula
  • Molecular Formula
  • Displayed Formula
  • Structural Formula
  • Skeletal Formula
  • 3D (Shape of Molecules)
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5
Q

Empirical Formula

A
  • Simplest ratio of the atoms of each element in a compound
  • Calculate by dividing the mass (or percentage given) by the atomic mass of each element to find the moles
  • Then divide the number of moles of each element by the smallest number calculated
  • Multiply out to get whole numbers if one comes out as a decimal
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6
Q

Molecular Formula

A
  • The actual number of atoms of each element in a molecule
  • Calculate the Mr of the empirical formula
  • Divide the Mr of the molecular formula by the Mr of the empirical formula
  • Multiply each atom in the empirical formula by the answer to step 2
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7
Q

Displayed Formula

A

Shows all the atoms and bonds in the molecule (single bonds, double bonds, triple bonds, etc)

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8
Q

Structural Formula

A

Shows the unique arrangement of atoms in a molecule in simplified form, without showing all the bonds

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9
Q

Skeletal Formula

A
  • Uses lines to show the bonds but don’t draw the carbons at all
  • The ends of the lines are carbon atoms (unless specified otherwise)
  • It is assumed there are the correct number fof hydrogen atoms on the carbons
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10
Q

3D Structures

A
  • Show how the model looks in 3D
  • Use a dashed line to show the atoms going away from us
  • Use a wedged line to show the atoms coming towards us
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11
Q

What system is used to name Organic Compounds?

A

IUPAC Systematic Naming Method

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12
Q

What does the root of the name show?

A

What the longest unbranched hydrocarbon is

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13
Q

What do suffixes show?

A

Functional Group

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14
Q

What do prefixes show?

A

Side chains or haloalkenes

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15
Q

Why do we number the longest chain?

A

The numbers for prefixes and suffixes show which number carbon the prefix or suffix is on in the longest chain

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16
Q

Isomers

A

Molecules that have the same molecular formula but different atom arrangements

17
Q

2 Types of isomerism

A
  • Structural isomerism
  • Stereoisomerism
18
Q

Types of Structural Isomerism

A
  • Position Isomerism
  • Functional Group Isomerism
  • Chain Isomerism
19
Q

Types of Stereoisomerism

A
  • Geometric/E-Z Isomerism
  • Optical Isomerism
20
Q

Structural Isomers

A

Same molecular formula but different structural formula

21
Q

Position Isomers

A
  • Same functional group but at different carbons on the chain
  • E.g Propan-1-ol and propan-2-ol
22
Q

Functional Group Isomers

A
  • Different functional groups
  • E.g. Ethanol and methoxymethane (an ether)
23
Q

Stereoisomerism

A

When 2 or more compounds have the same structural formula but different arrangements of atoms in space

24
Q

E-Z (Geometric) Isomerism

A

Restricted rotation around the double bond

25
Q

Z Isomers

A

The isomer with the priority groups on the same side of the double bond (AKA Cis)

26
Q

E Isomers

A

The isomer with the priority groups on opposite sides (AKA Trans)

27
Q

How can you identify priority groups?

A

The atom or compound that has the higher atomic number is the priority group

28
Q

When is there no E-Z isomerism?

A
  • When either carbon of the double bond has 2 of the exact same group on it
  • When there is no double bond
29
Q
A