Module 7 - Organic Chem Flashcards

(28 cards)

1
Q

What is a saturated compound?

A

Only contains single carbon bonds

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2
Q

What is an unsaturated compound?

A

Contains at least one double bond or triple bond between carbons.

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3
Q

What is an alkane

A

Contains only C and H, and only has single bonds

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4
Q

What is chloroalkane

A

contains C, H, and at least one CL

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5
Q

What is a Haloalkane

A

Contains C, H, nad at least one Halogen (F, Cl, Br, I)

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6
Q

What is a homologous series?

A

Contains molecules with properties that vary only slightly. Similar bonding structures, named similarly. e.g. Methane, Ethane, etc

Same/similar properities due to same/similar functional group

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7
Q

Alkanes reactivity

A

Least reactive due to single bond - low dispersion forces and non polarity. Thus insoluable in water.

saturated = harder to break the single bond.
More likely to substitute

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8
Q

Saturated Hydrocarbon

A

An Alkane

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9
Q

Unsaturated hydrocarbon

A

An alkene or an alkyne.

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10
Q

Alkene reactivity

A

Double bond makes them more reactive than alkanes.

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11
Q

Hydrogenation of Alkenes

A

Addition of hydrogen to carbon-carbon double bond.
- Removes the double bond
- Exothermic –> high activiation energy prevents it from taking place under normal conditions.

according to chem libre

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12
Q

Alkyne reactivity

A

Triple bond between carbons = very reactive except ethyne

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13
Q

What is an Isomer

A

Compound with the same molecular formula but different arrangement.
May be an alkane, alkene, alkyne but can’t tell with molecular formular

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14
Q

Types of isomers

A

Structural isomer, Stereoisomer (dont need to know this one tho)

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15
Q

What is a structural Isomer

A

Compound with same molecular formula but different bonding arrangement of atoms. Changing what is bonded to waht and where on the chain.
- Chain, position, functional group

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16
Q

What is a chain isomer

A

Structural isomer that arise due to different arrangements of their carbon skeleton.
straight chains or branched

17
Q

What is a position isomer

A

Structural Isomer made by moving the position of the functional group.

e.g. the double bond on the end, or in the middle of chain

18
Q

Functional group isomer

A

Structural isomer with compound with the same molecular formula but a different type of functional group.

  • Different homologous series
19
Q

Properties of Alkanes
- Type of bond between molecules
- polarity
-solubility in water
-Saturated or unsaturated?
-Main type of reaction

A

Disperson forces between molecules, non polar, insoluble in water, saturated, main type of reaction is substitution

20
Q

Properties of Alkenes
- Type of bond between molecules
- polarity
-solubility in water
-Saturated or unsaturated?
-Main type of reaction

A

Dispersion forces
non polar
Insoluable
unsaturated
Addition

21
Q

Properties of Alkynes
- Type of bond between molecules
- polarity
-solubility in water
-Saturated or unsaturated?
-Main type of reaction

A

Dispersion forces
nonpolar
insoluble
unsaturated
addition

22
Q

T/F

primary/secondary/tertiary alcohols can be considered structural position isomers

23
Q

T/F

Alcohols have a high boiling point- explain why

A

True - -OH group causes strong hydrogen bond and intermolecular bonding - thus higher boiling point. As the chain increases the dispersion forces increases and thus the boiling point also increases.

24
Q

What does the position of the OH group do to an alcohols boiling point?

A

In a primary - high boiling point
Secondary - lower boiling point
Tertiary - lowest boiling point.

  • in a tertiary alcohol the carbon atom attached to the OH group - strength of forces between atoms weaker
25
Define the solubility of alcohols
In small chains - alcohol is soluble due to the hydrogen bonds with water molecules. However in larger chains, solubility decreases. Alcohols do not disassociate to any specific extent in water and their solutions can be regarded as neutral.
25
Chemical reactions of Alcohols
Combustion - type of oxidation reaction involving oxidation Dehydration - type of elimination reaction where a double cc bond is formed by removal of H20. Substitution - changing in oxidation number. Primary alcohol - > aldehyde -> carboxylic acid secondary alcohols -> ketone Tertiary -> doesn't undergo oxidation Condensation- a reaction between an alcohol and a carboxylic acid in the presence of a catalust concentrated sulfuric acid to from an ester.
26
Describe boiling point of carboxylic acids
presence of hydrogen bonds e.g. COOH causes higher boiling point compared to the alkane of the same parent name. As chain increases the boiling point also increases.
27
What is the structure and physical properities of aldehydes and ketones
Double bond between 'C' and 'O' --> intermolecular bonds between molecules DO NOT FORM HYDROGEN BONDS as N,O,F NOT covalently bonded. They are polar tho and dipole-dipole attraction occurs between ketone molecules. Boiling point: highler boiling point than parent alkanes due to dipole-dipole attraction (stronger than dispersion) - so as chain increases, dispersion forces increases and boiling point increases. Solubility: can form hydrogen bonds in water - thus can disolve well in water - forms neutral solutions. when chain increases - solubility decreases due to distruption of hydrogen bonding between water molecules and non-polar hydrocarbon chains