organic compounds Flashcards

(27 cards)

1
Q

organic compounds

A

compound containing Carbon
except CO, Co2, H2Co3

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2
Q

four basic homologous series

A

alkanes
alkenes
alcohol
carboxylic acid

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3
Q

alkanes, alkenes
similarities

A

both hydrocarbons
- contain H, C
- mostly colourless

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4
Q

prefixes
C
C2
C3
C4
C5
C6

A

meth-
eth-
prop-
but-
pent-
hex-

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5
Q

alkanes v alkenes

A

alkanes
general formula: Cn H2n+2, n ≥ 1
functional group: none
end w/: -ane
saturated hydrocarbons

alkenes
general formula: Cn H2n, n ≥ 2
functional group: C=C
end w/: -ene
unsaturated hydrocarbons
more reactive, flammable than alkane cuz C=C more reactive, than C-C

prefixes are based on total no. of carbon

alkanes struct formula start w/ n = 1
alkenes struct formula start w/ n = 2

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6
Q

drawing struct formula important

A
  1. 1 carbon can ONLY take 4 bonds (4 sticks)
  2. if diagram ask copy down struct formula must place hydrogen, carbon at same place
  3. general formula for naming based on number of other “sticks” other than carbon.

I.e. C5h10br2 -ane (C5 and 12 other bonds)

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7
Q

alcohol, carboxylic acid common property

A

not hydrocarbons

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8
Q

alcohol properties

A
  1. funct grp —OH (hydroxyl)
  2. usally end w/ -anol (i.e. ethanol)
  3. Cn H2n+1 OH, where n ≥ 1
  4. all alcohol are neutral despite having O-H

alcohol struct formula start w/ n = 1

prefixes are based on total no. of carbon

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9
Q

carbolyxic/organic acid properties

A
  1. funct grp carboxyl
    C=O
    |
    O
    |
    H)
  2. usually end w/ -anioc acid
  3. Cn H2n+1 COOH, where n ≥ 0
  4. all weak acids

carboxylic acid struct formula start w/ n = 0

prefixes are based on total no. of carbon

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10
Q

wat to do w/ funct group

A

most times: add at end, struct formula

prefixes are based on total no. of carbon

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11
Q

all homologous series…

A

add Ch2 to get to next

i.e. methanol Ch4OH + Ch2 =
ethanol, C2h5Oh

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12
Q

how categorise into homologous series

A
  1. funct grp
  2. general form
  3. successive unit differ, Ch2 unit
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13
Q

4 reactions of alkanes

A
  1. incomplete combustion (insufficient o2)
  2. complete combustion (excess/enough o2)
  3. substitution w/ halogens (typically) (2 reactant form 2 products)
  4. Cracking
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14
Q

6 reactions, alkenes

A

combustion
1. incomplete combustion (insufficient o2)
2. complete combustion (excess/enough o2)

addition (2 reactants added, form one product)
3. hydrogenation (add hydrogen)
4. (halogen)nation (add halogen) (i.e. iodinisation)
5. hydration (add steam h2o(g))
6. addition polymerisation

https://docs.google.com/document/d/1Ep_FO9CxYSFbxmf3Zqg9mgm9NNyt2enpfMDr49gufrU/edit?tab=t.0 page 27 chlorinisation

https://docs.google.com/document/d/1Ep_FO9CxYSFbxmf3Zqg9mgm9NNyt2enpfMDr49gufrU/edit?tab=t.0 page 28 hydration

addition req C=C

Most, but not all addition reaction result in formation of alkanes.

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15
Q

hydrogenation reaction condition

A

Nickel as catalyst
200 deg celc

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16
Q

halogenation conditions

A

alkene, no condition for halogenation

alkane, req UV light, substitution

17
Q

hydrogenation conditions

A

300 deg celc
pressure 60 atm
phosphoric (V) acid as catalyst
steam (must be steam, not h2o (l)!)

300 + 60 + 5

hydration -> less letter, 200degcelc
hydrogenation -> more letter, 300 deg celc, 60 atm pressure, phosphoric (V)

18
Q

carboxylic acid reactions

A
  1. substitution w/ halogens (typically)
  2. Cracking

no combustion.

19
Q

incomplete combustion typically give out…

complete combustion typically give out…

A

incomp
CO, H2o, sometimes Carbon (soot)

comp
h2o, co2

20
Q

substitution of methane w/ chlorine gas (halogen)
visualise + what needed

A

https://docs.google.com/document/d/1Ep_FO9CxYSFbxmf3Zqg9mgm9NNyt2enpfMDr49gufrU/edit?tab=t.0 page 26

req UV light
one of hydrogen atoms, methane, replace by halogen atom

21
Q

as molecular mass of
4 homologous series compounds increase,

A

more carbon, stronger intermolecular forces
mp, bp increase
more viscous (more resistance, flow)

change of state gas -> liquid -> solid
density increase

flammability decrease EXCEPT
- Carboxylic acid not flammable (acid)
- Alkenes: %tage carbon increase, not molecular mass increase, causes decrease flammability

carboxylic acid does not undergo combustion

22
Q

what require for cracking reaction

A
  1. porous pot
  2. catalyst: Al2O3/SiO2
  3. high temp: at least 600deg celc
  4. room pressure: 1 atm
23
Q

cracking definition

A

break down of large alkane -> smaller hydrocarbon,
always producing alkene

24
Q

3 uses of cracking

A
  1. crack one of the components of fuel oil (mix of hydrocarbons) produce gasoline (petrol)
  2. crack alkenes produce plastic
  3. produce h2 (g)
25
alkanes properties
1. lowest mp, bp
26
what req for addition polymerisation
1. must contain funct grp: C=C bond (Carbon Carbon double bond) (saturated) ## Footnote saturated means contain C=C bond
27
how distinguish saturated from unsaturated hydrocarbon **IMPT**
add Br2 (aq) saturated hydrocarbon/alkane: - Br2 (aq) reddish-brown bromine remain reddish brown. - **substitution reaction, decolourises after very long period time** unsaturated hydrocarbon/alkene/contains C=C bond: - Br2 (aq) reddish-brown bromine decolourised rapidly - **addition reaction**