Unit 1 Flashcards

1
Q

Alkane/ ene/ yne polarity

A

Non polar

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2
Q

Alkane/ ene/ yne main intermolecular force

A

London dispersion

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3
Q

Alkane/ ene/ yne Mp/Bp

A

Low but get higher as the chain gets longer

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4
Q

Organic Halides polarity

A

More polar than hydrocarbons which means higher mp/ bp and more soluble. The more halogens there are, the more polar it gets

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5
Q

Alcohols polarity

A

Polar, they form hydrogen bonds so higher mp/ bp

Short chain alcohols are good polar solvents

Long chain alcohols are good polar and non polar solvents

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6
Q

Ethers polarity

A

Can not form hydrogen bonds but the oxygen makes it more polar than alkanes

Good as a polar and non polar solvent because it is very chemically stable

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7
Q

Aldehydes and ketones polarity

A

Both polar and non polar, good solvents. Less soluble in water that alcohol because there is no hydrogen bonding

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8
Q

Ethers mp/bp

A

Mp/ bp is higher than alkanes but lower that alcohols and water

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9
Q

Aldehydes and ketones mp/ bp

A

Lower than alcohols

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10
Q

Carboxylic acids polarity

A

Polar and form hydrogen bonds
Similar solubilities to alcohols
Behave like other acids

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11
Q

Carboxylic acids mp/bp

A

higher mp/bp than alcohols

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12
Q

Which side of esters goes first

A

Carboxylic acid

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13
Q

Ester polarity

A

Less polar than the parent acid and alcohol which leads to lower mp/ bp

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14
Q

Ester at room temp

A

Gasses. Lower molecular mass

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15
Q

Amines mp/bp

A

Higher than alkanes

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16
Q

Amines solubility

A

Smaller molecules are more soluble

17
Q

Amines smell

A

Fishy

18
Q

Amines Types of bonds

A

Hydrogen bonds

19
Q

Amines Bond polarity

A

Polar

20
Q

Amides properties

A

Weak bases, H+ receivers

21
Q

Amides solubility

A

Not soluble in water

22
Q

Amides Mp/ bp

A

If alkyl group is on the end they have lower mp/bp that if NH2 group is on the end

23
Q

Addition polymers

A

linkage by unsaturated carbon bonds

24
Q

Polyesters

A

Made from a dicarboxylic acid and a diol

25
Q

Polyamides

A

Made from an anime group and a carboxylic acid

26
Q

Alkanes substitution

A

Br2 turns into HBr

27
Q

Halogenation

A

Br2 breaks a double bond

28
Q

Hydrogenation

A

H2 breaks a bond (needs to be balanced)

29
Q

Hydrohalogenation

A

HBR breaks double bonds

30
Q

Hydration

A

H2O is used to form am alcohol

31
Q

Elimination (organic halides)

A

Strong acid or base is used to remove a halogen

32
Q

Dehydration (alcohols)

A

Alcohol turns into water and an alkene

33
Q

Condensation (ethers)

A

How an ether is formed

34
Q

Synthesis (A+K)

A

Aldehydes and keynote are formed

35
Q

Esterification

A

An ester is formed

36
Q

Hydrolysis/ saponificantion

A

A carboxylic acid and alcohol are formed from an ester

37
Q

Synthesis (amides)

A

Adding NH3 to a carboxylic acid

38
Q

Hydrolysis (amides)

A

Breaks them apart