C11 - organic chemistry Flashcards

(57 cards)

1
Q

define homologous series

A

family of similar compounds with similar chemical properties because of the same functional group
-physically slightly diff.

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2
Q

why does ane, ene, ol & oic acid react differently from each other but react similarly in the same homologues series

A

they have different functional groups. Compounds with similar functional groups have similar chemical prosperities

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3
Q

define saturated compound

A

compound with only single bonds

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4
Q

functional group of each homologues series

A

ane - only single covalent bond = saturated hydrocarbon compound
ene - 1 carbon carbon double bond (can be anywhere within the bond), cannot have for meth
ol - has 1 OH
oic acid - has 1 COOH
amine - NH2

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5
Q

define hydrocarbon

A

compound which contains only hydrogen and carbon

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6
Q

what type of reaction is with:
-ane
-ene

A

ane = substitution (swapping reaction) because ane has full bonds in every carbon so you swap the H
ene = addition

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7
Q

define alkanes

A

-saturated hydrocarbons molecules which contain only single covalent bonds
-generally unreactive, except in terms of burning

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8
Q

define alkenes

A

-unsaturated hydrocarbons whose molecules contain one double covalent bond

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9
Q

types of functional group surfix (name)

A

-ane
-ene
-ol
-oic acid
-amine

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10
Q

beginning names for naming compounds (uses no. Carbon) & their state in room temp

A

-meth (cannot for ene)
-eth (g)
-prop (g)
-but (g)
-pen (g)
-hex (l)
-hept (l)
-oct (l)
-non (l)

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11
Q

general formula for ane, ene, ol

A

ane - C n H 2n+2
ene - C n H 2n
ol - C n H 2n+1 OH
oic acid - C n H 2n+1 COOH

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12
Q

uses for all hydrocarbons

A

fuel

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13
Q

combustion reaction of hydrocarbons

A

incomplete - hydrocarbon + O2 -> CO or C (soot) + H2O
complete - hydrocarbon + O2 -> CO2 + H2O
-balance starting from C to H

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14
Q

reaction of ene to:
1) ane
2) ol

A

use a catalyst like Platinum/ Nickle
-break double bonds & join with H/ OH, all single bonds
1) react with H2 (hydrogenation)
ene + H2 -> ane
2) react with H2O (Steam) - break steam bond to H & OH (hydration)
ene + steam -> ol

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15
Q

test for unsaturated compound (ene)

A

-(halogenation)
-add Br2 (diatomic) to ene
-color changes from orange/ brown to colourless
(decolorizes Br2 solution)
-break double bonds & join with Br, all single bonds - break Br2 bond to Br & Br

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16
Q

fermentation reaction of glucose

A

C6 H12 O6 -> 2 C2 H5 OH + 2CO2
1 glucose -> 2 ethanol + 2 carbon dioxide
-anaerobic process
-uses yeast as catalyst & needs 25 -35C

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17
Q

2 uses of ethanol

A

-solvent
-fuel
(rubbing alcohol, cleaning wounds)

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18
Q

define Volatile

A

how easily it turns from liquid to gas

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19
Q

define viscous

A

how fluid (runny) a substance is
-shorter carbon chains = low viscosity
-longer carbon chains = high viscosity

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20
Q

define fossil fuel & its use

A

mixtures of hydrocarbons that formed from the remains of plants & animals from high temperature & pressure
-they’re combusted to generate electricity

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21
Q

types of fossil fuels

A

-petroleum (crude oil)
-coal
-natural gas, main constitute is methAne

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22
Q

define crude oil

A

-mixture of hydrocarbons which have different chain lengths

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23
Q

process of Fractional distillation of crude oil (petroleum)
evaporation & condensation

A

-oil is heated until evaporates into gas
-gases enter a column which is cooler at the top & hotter at the bottom
-gases start to cool & condense until it’s a liquid
-short chained hydrocarbons condense at the top, because of lower boiling points
-longer chained hydrocarbons condense at the bottom, because of higher boiling points
-hydrocarbons are separated into fractions

24
Q

order of fractions in crude oil fractional distillation from lowest boiling point & it use & state in room temp

A

-refinery gas = heating & cooking gas (g)
-petrol oil/ gasoline = fuel in motor vehicle (l)
-naphtha = feedstock for making chemicals (l)
-paraffin oil/ kerosene - fuel for aircrafts (l)
-diesel oil = fuel in diesel engine (l)
-lubricating oil = lubricating machinery (l)
-Fuel oil = fuel for marine engines/ heating (l)
-bitumen = road surfaces (l)

25
trends in Fractional distillation of crude oil (petroleum) as you go down
-contains diff types of anes in diff fractions -less volatility -more viscosity -heavier -increase in boiling point -longer chains -more molecular mass -more intermolecular forces -larger the molecule, more intermolecular forces, more energy needed to break them, higher melting/ boiling point
26
which hydrocarbons from crude oil are used mostly & what do you do with the ones not used
-the ones at the top -cracking the longer chained hydrocarbons
27
what properties of crude oil help it to separate
-diff chain lengths -diff boiling points
28
meaning of paraffin
anes, all of crude oils
29
process of cracking (ane to (ane) + ene + hydrogen) produced ene
-catalyst (zeolite) + heat (500C) -thermal decomposition -breaking long hydrocarbon chains into smaller hydrocarbon chains -alkane & alkene are produced -important because shorter chained hydrocarbons are more useful
30
cracking in the lab
-a test tube with porcelain chips & mineral wool soaked in paraffin with a tube leading into another test tube under water -heat the chips -insoluble gas is released
31
types of polymerization making macromolecule from many monomers
-addition -condensation
32
difference btw addition & condensation polymerization
-addition give 1 product, condensation gives 2 products -addition is made from same monomers, condensation is made from diff. monomers
33
why cannot alkanes become polymers
-they're saturated (only have single bonds) so they cannot form any extra bonds
34
define polymer
large molecules formed from many small units called monomers add ( ) n & bonds extending out of brackets to show it's a polymer eg. plastic
35
what are polymers
saturated compounds
36
define monomer (ene)
-a simple singular molecule -draw full bond & simplify it to this -bond: x can be either H or another compound x x \ / C (double bond) C / \ x x
37
define addition polymerization
monomers are added one to another & there's only 1 product -only for ene
38
polymer from addition polymerization
-only for ene -from monomer - break double bond & extend the bonds at the end -add ( ) n
39
examples of natural polymers naturally occurring
-natural rubber -protein -cellulose (in paper) -keratin (in hair)
40
examples of synthetic polymers (man made) made in lab
-polyester -polyamide -PVC (poly vinal chloride)
41
how is carbonic acid functional group drawn COOH (double to O, single bond to OH)
- O // C \ OH
42
how is amine functional group drawn NH2
- H / N \ H
43
define condensation polymerization
-react carboxylic acid with alcohol/ amine -gives 2 products; hydrocarbon & H20/ HCl/ NH3 -need double functional group so it can react on both ends
44
products of carboxylic acid &: -alcohol -amine
-ester + water -amide + water
45
reaction for carboxylic acid + alcohol
carboxylic acid + alcohol -> hydrocarbon + H2O ester link
46
reaction for carboxylic acid + amine
carboxylic acid + amine -> hydrocarbon + H2O amide link
47
how does an ester link form in singular functional group
-H from alcohol + OH from carboxylic acid = H2O -oxygen form alcohol bonds with C from carboxylic acid O || C - O - C - C (alcohol ) (carboxylic acid) -add ( ) n to make polymer
48
how does an amide link form in singular functional group
-H from amine + OH from carboxylic acid = H2O -N form amine bonds with C from carboxylic acid -(s) - single bond, (d) - double bond H O (s) (d) N ------ C (alcohol ) (carboxylic acid) -add ( ) n to make polymer | ||
49
how does polyester form in double functional group diol & dicarboxylic acid
-H from alcohol + OH from carboxylic acid = H2O -oxygen form alcohol bonds with C from carboxylic acid -for both sides -(s) - single bond, (d) - double bond - O O (d) (d) O - Carbons - O - C - Carbons - C -add ( ) n to make polyester | | || ||
50
how does polyamide form in double functional group (nylon) diamine & dicarboxylic acid
-H from amine + OH from carboxylic acid = H2O -oxygen form amine bonds with C from carboxylic acid -for both sides -(s) - single bond, (d) - double bond - H H O O (s) (s) (d) (d) N - Carbons - N - C - Carbons - C -add ( ) n to make polyamide
51
what is polythene
polymers made form ene eg. plastic
52
why is there no exact formula for the polymer molecules in polythene
polymer molecules contain a huge/almost infinite number of monomer units
53
what does nylon and polyamide have in common
they both have the same amide linkage
54
why reactions with hydrocarbons use a catalyst & the catalyst name
1) changing ene to ane/ ol: uses Nickle platinum catalyst 2) cracking uses Zeolite catalyst 3) fermentation of glucose uses yeast
55
note: when naming compounds, there may be a number in the middle = shows where the double bond is in the ene
56
note: -ane is generally unreactive -each carbon atom needs 4 bonds -ene cannot be for meth -ol is not a hydrocarbon, it is a carbohydrate, only ane & ene -paraffin from crude oil is used as fuel for aircrafts -never poly(ethane), always poly (ethEne) -diff bonds to an Ene have to be attached to the same C bond -all hydrocarbons can be used as a fuel -for ester/ amide link = acid - remove OH, amine/ ol - remove H -naming ester link = acid name + alcohol name eg. ethyl methanoate -naming amide link = acid name + amine name
57
explain why a reaction is exothermic
-bond breaking is endothermic -bond making is exothermic -more energy is given out in bond making than bond breaking so the reaction is exothermic