Unit 4 Flashcards

1
Q

Hydrocarbon?

A

Molecule with just carbons and hydrogens

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2
Q

Alkane?

A

Carbon and hydrogen only - saturated molecules

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3
Q

What intermolecular forces interact with alkanes?

A

Dispersion

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4
Q

What happens as the size of an alkane increases, in regards to its boiling point?

A

The larger the alkane, the increased strength and thus BP.

Larger =
- more atoms/surface area of interaction
- more electrons (which are dispersion forces)
- more dispersion
- INCREASE needed energy to break bonds
- Increase BP

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5
Q

What is dispersion forces?

A

Electrons orbit in each adjacent molecules, causing temporary dipoles

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6
Q

How do cyclic hydrocarbons similar to straight line carbon chains

A

similar chemical and physical properties

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7
Q

What can affect boiling point in alkanes?

A

Molar Mass (more electrons) thus heavier halogen has higher BP - (I > Br > Cl > F)
Branching
Size of ALKANE - length

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8
Q

How does branching in alkanes affect boiling point?

A

Molecules stack poorly against each other
Area of interaction smaller
LESS dispersion forces
LOWER (BP)

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9
Q

How does hydrogen bonding work and whats needed?

A

A H-FON bond within a molecule
- forming a partial charge (with partial negative on electronegative hydrogen FON)
- bonds with positive side on a hydrgeon on another atom

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10
Q

What does saturated mean in a hydrocarbon?

A

Saturated - single bonds, alkane, less reactive
Unsaturated - more than single bond (double, triple) - alkene, alkyne, more reactive

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11
Q

Which cyclocarbons are saturated vs unsaturated

A

Saturated - cycloalkane
Unsaturated - cycloalkene/alkyne

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12
Q

Whats Benzene?

A

C6H8
double bond every second carbon - but bond length/type in benzene are all the same
- electrons delocalise thus really stable
Hexagon with circle in middle (to represent delocalised electron cloud) located above and below the ring

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13
Q

Aromatic in QCAA?

A

Mean stuff like benzne
But also smelly stuff - esters

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14
Q

Saturated vs unsaturated as fuels

A

SATURATED
- single bonds only - stronger - more energy to break (thus release more energy which is what fuel is as) - thus alkanes and alchols

  • unsaturated have double/triple bonds - weaker - can lead to different products and potential of incomplete combustion - CO/soot
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15
Q

Why are alkanes used as fuels

A

Because they release energy well and smaller ones vaporise well (VOLATILITY)

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16
Q

What does volatile mean?

A

The ability to change from liquid to gas (vaporise) - at lower boiling points or smaller alkanes

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17
Q

How does alkane size affect flammability?

A

Smaller alkanes are more volatile as they vaporise quicker - liquid to gas

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18
Q

Complete combustion?

A

burn alkane in excess oxygen to form CO2 (carbon dioxide) and water
- keep in mind co2 is greenhouse gas

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19
Q

Simple Substitution

A

Replacing one species on molecule with another
I.e.
C2H5Br +HCL –> C2H5Cl + HBr
Haloalkane + hydrogen halide –> Haloalkane + hydrogen halide

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20
Q

Simple Condensation

A

When small molecule is lost in formation of a larger molecule + water
I.e.
CH3COOH + CH3OH –> CH3COOCH3 + H2O
methanoic acid (acetic acid) + methanol –> methyl ethanoate (methyl acetate)
Carboxylic Acid + Alcohol –> Ester

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21
Q

Simple Reduction

A

Species gain electrons
- when electromagnetic atom - like oxygen is removed from a molecule

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22
Q

Simple Addition

A

Joining 2/more molecules to form a larger molecule
C2H4 +H2 –> C2H6
Alkene + hydrogen –> alkane

23
Q

Simple Polymerisation

A

Joining many simple molecules to form a giant one
- reacting monomer molecules together in a chemical reaction to form polymer chain (polymers)

24
Q

Simple Elimination

A

Removing small group of atoms from a larger molecule C2H5OH –> C2H4 + H2O

25
Q

What mollecules can undergo addition?

A

Unsaturated molecules - double bond/triple broken to fit more atoms

26
Q

Simple Oxidisation

A

Species loses electrons (electronegative atom like oxygen is added to a molecule)

27
Q

Whats halogenation/type/condition if any?

A

Addition
Adding a halogen to generally a alkene forming a haloalkane
Alkene + Halogen –> dihaloalkane

ALKYNES
- same but form dihaloalkene –> tetrahaloalkane once do again

28
Q

What are halogens and which are commonly used

A

F, Cl, Br, I
Only Cl and Br usually
F - doesnt undergo addition well
I - less reactive

29
Q

Whats the way to memorise reductions vs oxidation and what it is

A

O xidation
I s
L ose
R eduction
I s
G ain

30
Q

Haloalkane?

A

Alkane with 1/more hydrogens replaced by halogen

31
Q

What type of reaction is alkene + halogen –> dihaloalkane?

A

addition - halogenation

32
Q

Whats hydrogenation and type/condition if any/any extra info?

A

Addition
Adding hydrogen to alkene forming alkane
Alkene + Hydrogen –> (platinum) –> alkane

ALKYNE:
just turns alkyne –> alkene –> alkane
(platinum)
alkyne –> alkene (and stay) needs lindlar catalyst

Condition:
platinum catalyst
H2 GAS presence

Also known as reduction as its the gain of atoms aka GAIN OF ELECTRONS
- saturating any carbon-carbon double bond

33
Q

Whats hydrohalogenation

A

Alkene + hydrogen halide
(addittion)

34
Q

What condition is needed for hydrogenation?

A

H2 gas
metal catalyst (normally platinum)

35
Q

What addition reactions require certain conditions and what are they?

A

Hydrogenation
(H2 gas and metal catalyst (normally platinum))

Hydration
(Steam for water, dilute aqueous acid as catalyst (H2SO4))

36
Q

What is hydration/type/condition if any?

A

Addition
Adding water moleucle to alkene to form an alcohol
Alkene + steam (water) –> (dilute acid/h2so4) –> alcohol

Condition:
Steam for water
Dilute acid like H2SO4

37
Q

Whats an alkyne

A

triple bond hydrocarbon C—C

38
Q

What condition is required for the halogenation or substitution with chlorine?

39
Q

Whats reduction in the context of addition

A

Hydrogenation or the gain of hydrogen atoms (electrons)
Since reduction is gain of electrons
(saturating any carbon-carbon double bond)

40
Q

Whats the functional group/prefix or whatever of carboxylic acid?

A

R - C – Double bond O (carbonyl group)
C - OH (hydroxyl)
RCOOH
-anoic acid

Derivative of aldehyde since adding an oxygen to it (oxidation) to get OH group

41
Q

Whats the functional group of ketone/prefix or whatever?

A

R-(C–O)-R
Carbonyl group in the middle of 2 R’s
-one

42
Q

Whats the functional group/prefix or whatever of amide?

A

R-CONH2
R-CONH-R
R-CON-R-R
Carbon double bond O
Same carbon - N - 2H/ or /HR/ or /RR,
R-C–O
C-N-(H2/RH/R2) -depednidng on prim, sec, tertiary
-amide
i.e. butanamide
butan-2-amide

43
Q

Whats the functional group/prefix or whatever of amine?

A

R-NH2
Functional: NH2
(can be NH1 with 2 R’s or just N with 3 R’s) changing to prim - sec - tertiary)
-amine
i.e. butylmine
butan-1-amine

44
Q

Whats the functional group/prefix or whatever of alcohol?

A

Hydroxyl group (OH)
R-OH
-anol
i.e. butanol
butan-1-ol

45
Q

Whats the functional group/prefix or whatever of aldehyde?

A

Like carboxylic acid (before) but with -H instead of -OH
R-CHO

R- C –O carbonyl group (O) Double bond
C - H

-anal
i.e. butanal
butan-1-al

46
Q

Whats the functional group/prefix or whatever of nitrile?

A

R-C—N (triple bond to C—N) basicly a cyanide
cyanide functional group

alkane-nitrile
i.e. butanenitrile
butan-1-nitrile

47
Q

Whats the functional group/prefix or whatever of alkyne?

A

C—C triple bond for hydrocarbon
yne
i.e. butyne

48
Q

atWhats the functional group/prefix or whatever of alkene?

A

C–C double bond hydrocarbon
ene
i.e. butene

49
Q

Whats the functional group/prefix or whatever of alkane?

A

C-C Single bond hydrocarbon
ane
i.e. butane

50
Q

Whats the functional group/prefix or whatever of ester?

51
Q

Whats the functional group/prefix or whatever of ether?