Organic Chemistry Flashcards

(61 cards)

1
Q

What are all the Reactions of Alkanes

A
  • Cracking
  • Combustion
  • Chlorination and Bromination (substitution)
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2
Q

Cracking of Alkanes

A

Alkane -heat/catalyst——> Smaller Alkane + Smaller Alkene

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3
Q

Combustion of Alkanes

A

Alkane + O2 —ignite excess oxygen—> CO2 + H2O

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4
Q

Chlorination/ Bromination of Alkanes

A

Alkane+ X2 —–UV Light Energy —-> Haloalkane +HX

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5
Q

All Reactions of Alkenes

A
  • Alkene + Hydrogen Halide —-> Haloalkane
  • Alkene —-Acidified H2O —–> Alcohol
  • Alkene + X2 —-> Dihaloalkane
  • Alkene —-H2—–Pt—> Alkane
  • Alkene —-Acidified MnO4- —-REFLUX—–> di-ol
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6
Q

MP/BP of Alkanes

A

bonded by weak intermolecular forces and are non polar, thus low MP, longer the chain, the higher the mp due to stronger bonds between molecules.

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7
Q

MP/BP of Alkenes

A

bonded by weak intermolecular forces and are non polar, thus low MP, longer the chain, the higher the mp due to stronger bonds between molecules.

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8
Q

Solubility of Alkanes and Alkenes

A

Insoluble in Water due to being non polar molecules. Compared to H2O which has slightly negative O and Slightly positive H, so they are not soluble and it is immiscible with water forming two separate layers. Smaller Chain Alkanes are less dense than water and will float on top

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9
Q

Alkene + Hydrogen Halide

A

Addition Reaction Alkene + Hydrogen Halide —> Haloalkane (Markovniks Rule)

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10
Q

Alkene —-Acidified H2O->

A

Addition Reaction Alkene —-Acidified H2O —–> Alcohol (Markovniks Rule)

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11
Q

Alkene + X2 —->

A

Addition Reaction Alkene + X2 —-> Dihaloalkane (Markovniks Rule)

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12
Q

Alkene —-H2—–Pt-heat—->

A

Alkene —-H2—–Pt—> Alkane Addition Reaction (Markovniks Rule)

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13
Q

Alkene —-Acidified MnO4- —-REFLUX—–>

A

Oxidation Reaction Alkene —-Acidified MnO4- —-REFLUX—–> di-ol

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14
Q

Alkene —-heat/Dilute H2sO4—–>

A

Alkene —-heat/Dilute H2sO4—–> Alcohol

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15
Q

why mp/bp increase alkene and alkane chain length

A

molar mass increases, larger the molar mass, more total valence electrons available, which can randomly cluster to one side of the molecule making an instantaneous polar end - thereby creating a stronger bond to another molecule’s instantaneous polar end

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16
Q

comparison of alkane and alkene mp/bp

A

each alkene has 2 fewer electrons than the alkane counterpart, thus decreasing the strength in the molecular bonds which decreases the bp of alkenes

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17
Q

requirements for cis trans isomerism

A

C=C Double Bond (or ring structure):
Prevents rotation, allowing for fixed positions of substituents.

Each carbon of the double bond must have two different groups attached:

If either carbon has two of the same groups, cis–trans isomerism is not possible.

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18
Q

why geometric isomerism

A

Unlike single bonds, double bonds cannot freely rotate, due to the rigid π (pi) bond. This fixed shape allows different spatial arrangements to be “locked in.”

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19
Q

Alkene —Monomers+heat+catalyst+pressure—>

A

Alkene —Monomers+heat+catalyst+pressure—>Polymer

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20
Q

Alkene —H+/MnO4- (reflux) —->

A

Alkene —H+/MnO4- —-> Diol

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21
Q

Haloalkane —-NH3+heat——>

A

Haloalkane —-NH3+heat——> Amine

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22
Q

Amine Acid or Base

A

Base
- Turns red litmus blue
turns green UI blue

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23
Q

Haloalkane—–KOH(alc)+heat—->

A

Haloalkane—–KOH(alc)+heat—-> Alkene

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24
Q

Haloalkane —KOH(aq)+heat—->

A

Haloalkane —KOH(aq)+heat—-> Alcohol

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25
Haloalkane-> Alcohol
Haloalkane ---KOH(aq)+heat----> Alcohol
26
Haloalkane-> Alkene
Haloalkane-----KOH(alc)+heat----> Alkene
27
Haloalkane -> Amine
Haloalkane ----NH3+heat------> Amine
28
Alkene-> Diol
Alkene ----Acidified MnO4- ----REFLUX-----> Diol
29
Alkene ---> Alcohol
Alkene---H2O/H+,heat----> Alcohol
30
Alkene->Dihaloalkane
Alkene+X2---->Dihaloalkane
31
Alkenes ---> Polymer
Alkene---heat+pressure+catalyst+monomers---> Polymer
32
Alkenes ---> Alkanes
Alkenes----H2----Pt, heat---Alkane
33
Alkenes ----> Haloalkane
Alkene +HX -----> Haloalkane
34
Alkanes--->Haloalkane
Alkane +X2 -----UV light/heat----> Haloalkane
35
Alcohol ----Conc. H2sO4--->
Alcohol ----Conc. H2sO4--->Alkene
36
Alcohol----> Alkene
Alcohol ----Conc. H2sO4--->Alkene
37
Alcohol---MnO4-/H+ (heat)--->
Alcohol---MnO4-/H+ (heat)--->Carboxylic Acid
38
Alcohol---> Carboxylic Acid
Alcohol---MnO4-/H+ (heat)--->Carboxylic Acid
39
Alcohol----SOCl2/PCl5/PCl3---->
Alcohol----SOCl2/PCl5/PCl3----> Haloalkane
40
Alcohol--->Haloalkane
Alcohol----SOCl2/PCl5/PCl3----> Haloalkane
41
Carboxylic Acid/Base
Acid - blue litmus ->red - UI from green to orange
42
Alcohol Polarity
Smaller Alcohols are very polar as the difference in electronegativity between the O-H bond is very high. However polarity gets weaker with chain length
43
Alcohol Solubility
- Smaller- Soluble due to high polarity - Larger- Weaker due to lower polarity
44
Alcohol B.P
Tends to be Higher than other organic compounds due to the presence of the polar OH group, which makes intermolecular forces stronger. Increases w/ chain length
45
Amine Solubility
- Lower chain amines have higher solubility due to the polar N-H bonds
46
RNH2+H2O (Amine + Water) --->
RNH2+H2O--->RNH3+ + OH- (alkylammonium ion+hydroxide ion)
47
Amine+Acid--->
Alkylammonium___ ion + Water
48
Carboxylic Acid+Metal
Carboxylic Acid+Metal-> Metal Salt (ethanoate) + H2
49
Carboxylic Acid + Water
Carboxylic Acid + Water----> -anoate ion + H3O+
50
Carboxylic Acid + Carbonate (Weak base)
Carboxylic Acid + Carbonate (Weak base)---> Carboxylic Salt+CO2+Water
51
Carboxylic Acid + Base
Carboxylic Acid + Base ---> Carboxylic Salt+ H2O
52
Carboxylic Acid + Amine
Carboxylic Acid + Amine ---> ---- alkylammonium -anoate salt + water
53
Carboxylic Acid B.P
- High B.P , due to functional group, increases with chain length.
54
Carboxylic Acid Miscibility with Water
<10 completely miscible in water due to formation of H bonds with water.
55
Carboxylic Acid Polarity
- Polar as smaller molecules, but non polar as larger molecules
56
B.P of Haloalkanes
- higher than hydrocarbons due to the halogen group attached - Increases with chain length
57
Solubility of Haloalkanes
- Slightly soluble in water - relatively large amount of energy required to break bonds between halogen and carbon -smaller amount of energy released when bond is formed w/ water.
58
Polymer reactivity
- unreactive compared to monomers due to the single C-C bonds being less reactive than the C=C double bonds.
59
when being reduced, what color does MnO4- turn into
purple->colourless
60
when being reduced, what color does dichromate turn into
orange---> green
61
functional group priority
Carboxylic Acid Alcohol Amine Alkene Alkyne Haloalkane Alkane