AS Chemistry必背的51个定义(CAIE 9701)

CAIE AS Chemistry(9701)考试涉及到的定义还是比较多的,本身掌握定义也是熟练掌握和运用知识点的第一步,大家不妨把背定义放在复习的第一步完成。

今天为大家总结AS考试必备、必背的51个定义!

1Relative atomic mass

The weighted mean/average mass of an atom relative to 1/12 the mass of an atom of C-12

02Relative isotopic mass

Mean/average mass of an atom relative to 1/12 the mass of an atom of C-12

03Relative molecular mass

Mean/average mass of an molecule relative to 1/12 the mass of an atom of C-12

04Relative formula mass

Mean/average mass of an molecule relative to 1/12 the mass of an atom of C-12

05Isotope

Atoms with the same number of protons and different number of neutrons

06Atomic number

Proton number or number of protons

07Mass number

Nucleon number; total number of protons and neutrons

08First ionisation energy

The amount of energy required to remove one electron from each atom in one mole of atoms of the element in the gaseous state (to form gaseous 1+ ions).

09Ionic bonding

Attraction/attractive force between positively and negatively charged ions in an ionic lattice.

10Covalent bonding

Attraction between nucleus and shared pair of electrons.

11Dative covalent bonding

One atom provides both electrons in the formation of the covalent bond.

12Sigma bond (σ bond)

Sigma bonds are formed by end-on overlap of atomic orbitals.

13Pi bond (Π bond)

Pi bonds are formed by sideways overlap of p-type atomic orbitals.

14Standard conditions

100kPa and 298K

15Enthalpy change of formation

The enthalpy change when one mole of a compound is formed from its elements

16The standard enthalpy change of formation

The enthalpy change when one mole of a compound is formed from its elements under standard conditions.

17The standard enthalpy change of combustion

The enthalpy change when one mole of a substance is burnt in excess oxygen under standard conditions.

18The standard enthalpy change of atomisation

The enthalpy change when one mole of gaseous atoms is formed from the element in its standard state under standard conditions.

19The standard enthalpy change of neutralisation

The enthalpy change when one mole of water is formed by the reaction of an acid with an alkali under standard conditions.

20The standard enthalpy change of solution

The enthalpy change when one mole of solute is dissoved in a solvent to form an infinitely dilute solution under standard conditions.

21The standard enthalpy change of hydration of an anhydrous salt

The enthalpy change when one mole of hydrated salt is formed from one mole of the anhydrous salt under standard conditions.

22Hess's law

The total enthalpy change in a chemical reaction is independent of the route by which the chemical reaction takes place as long as the initial and final conditions are the same.

23Bond enthalpy

The total amount of energy required to break 1 mole of that chemical bond.

24Reduction

Reduction is gain of electrons

Reduction is a decrease in oxidation number

25Oxidation

Oxidation is an increase of oxidation number.

Oxidation is loss of electrons.

26Equilibrium

It is dynamic.

The forward and reverse reactions occur at the same rate (of reaction).

The concentrations of reactants and products remain constant at equilibrium

It requires a closed system

27Le Chatelier's principle

If one or more factors that affect an equilibrium is changed, the position of equilibrium shifts in the direction that reduces (opposes) the change.

28Bronsted-Lowry acid

A Bronsted-Lowry acid is a proton donor

29Bronsted-Lowry base

A Bronsted-Lowry base is a proton acceptor

30Strong acids

Acids that dissociate almose completely in solution are called strong acid.

31Weak acids

Acids that are only partially dissociated in solution are called weak acid.

32Strong base

Bases that dissociate almost completely in solution

33Weak base

Weak Bases which dissociate to only a small extent in solution

34Activation energy

The minimum energy that colliding particles must possess for a successful collision to take place.

35Catalyst

A substance that increases the rate of a reaction but remains chemically unchanged itself at the end of the reaction.

36Amphoteric

Compounds that can act as both acids and bases, such as aluminium oxide.

37Group 2 metal

The group 2 metals get more reactive going down the group

38Group 17 halogens

The halogens (Cl2,Br2,I2molecules) get less reactive going down Group 17.

More reactive halogen can displace a less reactive halogen from a halide solution of the less reactive halogen.

39The hydrogen halides

(HF, HCl, HBr, HI)

The hydrogen halides get less thermally stable going down group 17

HF least thermally stable

HI most thermally stable

It gets easier to oxidise the hydrogen halides going down group 17.

40Halogenoalkane

(R-Cl; R-Br; R-I)

Halogenoalkane becomes more reactive down the group

Fluoroalkanes least reactive

Iodoalkanes most reactive

41Disproportionation

The element chlorine (Cl2) undergoes a type of redox reaction called disproportionation when it reacts with alkali.

self reduction and oxidation

the actual reaction that takes place depends on the temperature.(in cold/hot alkali)

42Structural isomers

Structural isomers have the same molecular formula but different structural formulae.

43Stereoisomerism

Molecules have the same atoms bonded to each other but with different arrangements of the atoms in space.

44Optical isomerism

If a molecule contains a carbon atom that is bonded to four different atoms or groups of atoms, it can form two optical isomers. The two different molecules are mirror images of each other and cannot be superimposed.

45Chiral centre

The carbon atom with the four different groups attached.

46Free radicals

Free radical has an unpaired electron.

It is very reactive and produced when a bond breaks homolytically. (homolytic fission)

47Heterolytic fission

A bond breaks unevenly to form ions.

48Carbocation

Positive alkyl ion

49Nucleophile

A donator of a pair of electrons

50Electrophile

An acceptor of a pair of electrons

51Positive inductive effect

The electron-donating nature of alkyl groups has a positive inductive effect on adjacent groups.

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