• Shuffle
    Toggle On
    Toggle Off
  • Alphabetize
    Toggle On
    Toggle Off
  • Front First
    Toggle On
    Toggle Off
  • Both Sides
    Toggle On
    Toggle Off
  • Read
    Toggle On
    Toggle Off
Reading...
Front

Card Range To Study

through

image

Play button

image

Play button

image

Progress

1/52

Click to flip

Use LEFT and RIGHT arrow keys to navigate between flashcards;

Use UP and DOWN arrow keys to flip the card;

H to show hint;

A reads text to speech;

52 Cards in this Set

  • Front
  • Back
Structural isomer
same molecular formula, different structure
Hydrocarbon
a compound that contains hydrogen and carbon only
Saturated
contains only single C-C bonds
Radical
species with an unpaired electron
Fractional distillation
separates due to differences in boiling point
Fraction
mixture of compounds of similar boiling point
Cracking
breaking a long chain alkane into a shorter chain alkane and an alkene
Fuel
a substance that is burned to produce heat
Biofuel
a fuel produced from plant or animal waste
Stereoisomer
same structural formula but different arrangement in space
E/Z isomers
isomers resulting from restricted rotation about a double bond, where two different groups are attached to each carbon of the C=C
Unsaturated
contains one or more C=C bond
Electrophile
electron pair acceptor
Nucleophile
lone pair donor
Reflux
continuously boil and condense
Standard conditions
Temperature 298K, pressure 101 kPa, 1moldm3
Enthalpy change of reaction
Enthalpy change when the reaction occurs in the molar quantities shown in the chemical equation
Enthalpy change of formation
Enthalpy change when one mole of a compound is formed from its elements
Enthalpy change of combustion
Enthalpy change when one mole of a substance undergoes complete combustion
Hess’s Law
Total enthalpy change is independent of route
Average bond enthalpy
Energy needed to break one mole of gaseous bonds
Activation energy
Minimum energy needed for a reaction to occur
Catalyst
increases rate of reaction without being consumed by overall reaction
Le Chatelier’s Principle
When the conditions on a system in equilibrium are changed, the position of equilibrium shifts to minimise the change
Dynamic equilibrium
Rates of forward and backward reactions are equal
why straight chain isomers higher bp than branched?
branched chains have less surface contact therefore weaker Van der Waals forces
how is ozone concentration maintained?
O2 + O ↔ O3
why is ozone important to life on earth
absorbs harmful UV
why increasing concentration increases rate of reaction
more crowded particles means more collisions per second
how catalysts increase rate of reaction
activation energy is lowered more molecules have enough energy to react
how high temp increase rate of reaction
activation energy does not change more molecules have enough energy to react
atom economy equation
(mass of desired product/mass of all products) x 100
how to reduce environmental damage from disposal of polymers
Develop photodegradable or biodegradable polymers. Develop ways to sort and recycle polymers
why alcohols soluble in water
has hydroxyl group so forms hydrogen bond with water
bond ____ releases energy
forming
bond ____ absorbs energy
breaking
exothermic enthalpy change
more energy released than absorbed (negative value)
endothermic enthalpy change
more energy absorbed than released (positive value)
enthalpy change units
kJmol⁻¹
homologous series
Series having same functional group and a general formula
percentage yield equation
(actual mol product/theorectical mol product) x 100
effect of absorption of infrared radiation on bonds between molecules
vibrate more
environmental problem of NO
causes photochemical smog. depletes ozone
environmental problem of CO
toxic (reduces capacity of blood to carry oxygen)
primary alcohol + acidified dichromate ions (heat and distil)
aldehyde
primary alcohol + acidified dichromate ions (reflux)
carboxylic acid
alcohol + carboxylic acid (acid and heat)
ester
secondary alcohol + acidified dichromate ions (heat reflux)
ketone
tertiary alcohol + acidified dichromate ions
no reaction
If alcohol is oxidised, acidified K₂Cr₂O₇ changes from
orange to green
alkene + steam (heat and acid)
alcohol (hydration)
alcohol + conc. acid (heat)
alkene + water (elimination)