Introduction to organic chemistry Flashcards

1
Q

Define the term molecular formula

A

Formula showing the actual number of atoms of each element in a molecule

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2
Q

Define the term empirical formula

A

Formula showing the smallest whole number ratio of atoms in a compound

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3
Q

Give the empirical formula of the compound C6H1206

A

C2H402

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4
Q

Define the term structural formula

A

Formula showing the arrangement of atoms in a compound carbon by carbon

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5
Q

Give the structural formula of the compound pentane

A

CH3CH2CH2CH2CH3

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6
Q

Define the term displayed formula

A

Shows how atoms are arranged and the bonds between them

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7
Q

Define the term general formula

A

An algebraic formula that can describe any member of a family of compounds

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8
Q

Define the term Homologous series

A

A family of compounds that Have the same functional group and general formula

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9
Q

List 3 characteristics shared by members of the same homologous series

A

They show a gradual change in physical properties
They have the same chemical properties
Each member of a homologous series differs by CH2 from the last member

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10
Q

Give the general formula of alkanes

A

CnH(2n+2)

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11
Q

Are alkanes saturated or unsaturated?

A

Saturated

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12
Q

Define the term saturated

A

Each carbon Atom has made four bonds so it’s impossible to make more

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13
Q

Give the general formula of cycloalkanes

A

CnH2n

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14
Q

Are cycloalkanes saturated or unsaturated?

A

Saturated

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15
Q

State the prefix and suffix of a cycloalkane

A

Prefix: cyclo
Suffix: ane

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16
Q

Give the general formula for branched alkanes

A

CnH2n+2

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17
Q

What is the group name for branches?

A

Alkyl

18
Q

Give the general formula of alkenes

A

CnH2n

19
Q

Are alkenes saturated or unsaturated?

A

Unsaturated

20
Q

Define the term unsaturated

A

The carbon atoms on either end of the double bond or bonded to three atoms each so they could form another bond

21
Q

Give the general formula for alcohols

A

CnH(2n+1)OH

22
Q

Give the general formula for aldehyde

A

R-CHO

23
Q

What does “R” represent?

A

An alkyl group or a hydrogen Atom

24
Q

Give the general formula for ketones

A

R-CO-R’

25
Q

Give the general formula for carboxylic acids

A

R-COOH

26
Q

Define the term nomenclature

A

Naming molecules containing carbon using rules

27
Q

Identify the steps involved in naming a molecule

A
  1. identify the longest chain of carbons. This gives you the stem name
  2. Identify any branches and/or functional groups
  3. Numbered the main carbon chain so the highest priority functional group has the lowest number possible
  4. The highest priority functional group takes the suffix
  5. If you have more than one of the same type of functional group then use di/tri/tetra (Eg: dichloro)
  6. If you have more than one of the same type of functional group then put them in alphabetical order (Eg: bromo before chloro)
28
Q

Identify the steps involved in naming cycloalkanes

A
  1. count the number of carbon atoms in the ring
  2. add the prefix cyclo and suffix ane
  3. If any alkyl groups are attached just add the alcohol prefix without a number . If there’s more than one alkyl group give the alkyl group that’s alphabetically first the lower number
29
Q

Define the term structural isomer

A

Compounds with the same molecular formula but different structural formula

30
Q

Name three tripes of structural isomers

A

Chain isomers
Position isomers
Functional group isomers

31
Q

What are chain isomers

A

Isomers with the same functional group but different arrangement of the carbon skeleton

32
Q

What are position isomers

A

Isomers which have the same skeleton atoms/groups of atoms but the atoms/groups of atoms are attached to different carbon atoms

33
Q

What are functional group isomers?

A

Buy some hoes which all have the same type and number of atoms but they are arranged into different functional groups

34
Q

What are stereoisomers?

A

Isomers with the same structural formula but their atoms are arranged differently in space

35
Q

The carbon atoms in a carbon-to-carbon double bond and the atoms bonded to them lie in the same…

A

plane

36
Q

When do you get E/Z isomerism?

A

when the two carbon atoms involved in the carbon-to-carbon double bond each have two different atoms or groups of atoms attached to them (they don’t have to be different to the ones on the opposite carbon atom)

37
Q

if the two groups of atoms or opposite to each other what type of isomer is it?

A

An E isomer

38
Q

If they are both above or below what type of isomer is it?

A

A Z isomer

39
Q

If The carbon atoms Have two different groups attached how do you judge if it’s an E or Z isomer?

A

By seeing if the highest priority groups are on the opposite sides or the same side

40
Q

List the steps needed to identify what type of isomer it is if all four groups are different

A

List the steps needed to identify what type of isomer it is if all four groups are different
1. Consider the groups joined to the right hand side of the carbon carbon double bond
Considered the atomic number of the atoms attached
Whichever has the higher atomic mass takes priority
If they are the same then consider atoms one bond further away
2. Consider the groups joined to the left hand side of the carbon to carbon double bond
Consider the atomic mass of the atoms attached
Whichever has the greater atomic mass strakes priority
3. If the highest priority groups are on opposite sides then it is an E isomer. If they are on the same side than it is a Z isomer