(🟠 TOPIC 1) Key Definitions … Flashcards

1
Q

Atomic number (z)

A

The number of protons in the nucleus of an atom of a certain element

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2
Q

Mass number (A)

A

The sum of the number of protons and the number of neutrons in the nucleus of an atom of a certain element

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3
Q

Isotopes

A

An atom of the same element with the same number of protons, but a different number of neutrons, therefore a different mass number
(Isotopes of the same element have identical chemical properties because they have identical electronic configurations)

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4
Q

Relative atomic mass (Ar)

A

The weighted mean mass of an atom of an element relative to 1/12th of the mass of an atom of carbon-12 which has a mass of 12

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5
Q

Relative isotopic mass

A

The mass of an atom of an isotope of an element relative to 1/12th of the mass of an atom of carbon-12 which has a mass of 12

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6
Q

m/z

A

Mass to charge ratio
In mass spectrometry, nearly all ions will have lost one electron, making them +1 ions, but …
If a 2+ ion is formed, m/z = m/+2, so the m/z value is halved

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7
Q

Molecular ion peak (/parent ion peak)

A

The peak with the highest m/z ratio in the mass spectrum (the M peak). This gives the Mr of the whole molecule.
(It is the last peak (apart from the M+1 peak if visible - very small))
However, the molecular ion peak is also sometimes quite small

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8
Q

Orbital

A

A region of space within an atom where there is a high probability of finding an electron. It can hold up to two electrons with opposite spins.
(Orbitals increase in size as they move further away from the nucleus (higher quantum shells))

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9
Q

Aufbau Principle

A

Type of electronic configuration notation (s,p,d,f)
Subshells of lowest energy are filled first

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10
Q

Hund’s Rule

A

States that electrons will occupy the orbitals singly before pairing takes place.
Type of electronic configuration notation (s,px,py,pz…)
(Eg. P orbital on the x-plane/ axis)

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11
Q

Pauli Exclusion Principle (box notation)

A

States that two electrons cannot occupy the same orbital unless they have opposite spins.
Type of electronic configuration notation (boxes with half arrows - up,down)

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12
Q

Periodicity

A

The repeated trend in properties across a period
(Electronic configurations, atomic radii, melting + boiling temperatures, first ionisation energy)

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13
Q

Atomic radius

A

Distance from centre of nucleus to boundary of electron cloud

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14
Q

Quantum shell

A

Defines the energy level of an electron.
Electrons in the first quantum shell/energy level have the lowest energy (energy of electrons increases as they go further away from the nucleus)

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15
Q

S-block element

A

Has highest energy electron in an s-orbital

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16
Q

P-block element

A

Has highest energy electron in a p-orbital

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17
Q

D-block element

A

The d-sub shell is being filled
(Cannot be defined in same way as other blocks as the 4s subshell will be filled before the 3d subshell, so has more energy than the 3d subshell. Therefore the highest energy electron is not in the d subshell)

18
Q

What’s the difference between relative molecular mass and relative formula mass?

A

Relative molecular mass is the sum of Mr of simple molecules (eg. N2, H2SO4)
Relative formula mass is the sum of Mr of compounds with giant structures (eg. Pb(NO3)2)

19
Q

M+1 peak

A

A very small peak that sometimes occurs after the M-peak - caused by the presence of carbon-13 (isotopes)

20
Q

Base peak

A

The tallest peak, the most abundant molecule/atom in a sample

21
Q

Isomer

A

Compounds with the same molecular formula but with a different arrangement of atoms in the molecule and different properties

22
Q

Geometric isomerism

A

Compounds with a C=C double bond with atoms/ groups attached to it at different positions (E/Z, cis/trans)

23
Q

Crude oil

A

A mixture of mostly alkanes of different chain lengths and therefore different boiling points

24
Q

Cracking

A

The process of breaking excess heavier hydrocarbons into smaller, more useful compounds
Large alkane —> Smaller alkane + alkene (with aluminium oxide catalyst Al2O3)

25
Q

Reforming

A

Converting straight chain hydrocarbons into branched and/or cyclic hydrocarbons for efficient combustion

26
Q

Carbon neutral

A

No NET release of carbon dioxide into the atmosphere (eg. The rate of carbon released from combustion = to the rate of carbon dioxide taken in by plants through photosynthesis)

27
Q

Heterolytic fission

A

Unequal sharing of the electrons in the covalent bond when it breaks to form one +ve ion and one -ve ion (both electrons shift to one of the atoms - shown by full arrow head)

28
Q

Homolytic fission

A

Equal sharing of the electrons in the covalent bond when it breaks, resulting in free radicals (shown by half arrow heads)

29
Q

Sigma bond

A

A covalent bond formed when electron orbitals overlap end-on (stronger)

30
Q

Pi bond

A

A covalent bond formed when electron orbitals [p-orbitals] overlap sideways (weaker) forming two regions of negative charge (above and below the sigma bond)
Note: a double bond is made up of a sigma bond and a pi bond

31
Q

Electrophile

A

An electron PAIR acceptor
—> An electron-deficient chemical compound (or atom) that is attracted to electrons and tends to accept pairs of electrons (eg. Positive ion, delta +)

32
Q

Carbocation

A

An ion with a positively charged carbon atom within in

33
Q

Primary carbocation

A

The carbon with the positive charge is bonded to only one other carbon (least stable)

34
Q

Secondary carbocation

A

The carbon with the positive charge is bonded to two other carbon atoms (more stable)

35
Q

Tertiary carbocation

A

The carbon with the positive charge is bonded to three other carbon atoms (most stable).

36
Q

Markovnikov’s Rule

A

In electrophilic addition, the H (or Br/Cl for diatomic) (ie. The first atom of the molecule to bond), will bond to a carbon so that the most stable carbocation can form (ie. Joins to the carbon with the least carbons attached)
This will form the major product. A minor product is formed when the most stable carbocation is not formed.

37
Q

Primary halogenoalkane

A

The carbon which carries the halogen atom is only attached to one other carbon atom (same concept for secondary and tertiary)

38
Q

Nucleophile

A

An electron PAIR donor
—> an atom/ion with a lone pair, (or delta -) which is attracted to areas of slightly positive charge or electron deficient atoms

39
Q

Hydrolysis

A

Breaking up a substance using water (eg. Nucleophilic substitution with OH-)

40
Q

Nucleophilic substitution

A

A reaction in which an attacking nucleophile replaces an existing atom or group in a molecule

41
Q

Elimination reaction

A

A reaction in which a molecule loses atoms (H and X) attached to adjacent carbon atoms forming a C=C double bond. (The OH- acts as a base, not a nucleophile in this case)

42
Q

Infrared spectroscopy

A

The process of using infrared radiation to determine certain bonds present and therefore the functional group. The bonds absorb the radiation causing them to vibrate