Introduction to Organic Flashcards

1
Q

How to show the displayed formula

A

All bonds are shown with double or triple bonds

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2
Q

How to show the structural formula

A

Each carbon is written separately with atoms or groups attached to each

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3
Q

How to show the skeletal formula

A

Straight lines used for carbon-carbon bonds, hydrogens ignored. Extra molecules are written on ends of lines

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4
Q

Example of alkane

A

Ethane

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5
Q

Example of alkene

A

Ethene

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6
Q

Functional group and example of haloalkane

A

R-X, bromoethane

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7
Q

Functional group and example of alcohol

A

R-OH, ethanol

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8
Q

Functional group and example of aldehyde

A

R-CHO, ethanal

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9
Q

Functional group and example of ketone

A

R-CO-R, propanone

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10
Q

Functional group and example of carboxylic acid

A

R-COOH, ethanoic acid

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11
Q

Types of structural isomers

A

Positional, functional, chain

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12
Q

What is positional isomerism

A

Position of functional group is changed

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13
Q

What is functional isomerism

A

Functional group is changed

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14
Q

What is chain isomerism

A

Longest carbon chain is changed

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15
Q

Define structural isomerism

A

Same molecular formula, but different structural formula

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16
Q

Define stereoisomerism

A

Same structural formula, but different spacial arrangement

17
Q

What is E-Z isomerism

A

Form of stereoisomerism, due to restricted rotation of carbon-carbon double bond

18
Q

How to do E-Z isomerism

A

If higher property atoms are on the same side, it’s Z.

If on different sides, it’s E.

19
Q

How to select which atom is higher property

A

The atom which has the higher atomic number is given the higher priority

20
Q

What are straight chain isomers

A

Isomers with all carbons in the longest chain