atomic structure Flashcards

1
Q

what is an atom?

A

an atom is the smallest component of an element having the chemical properties of the element.
all atoms are made up of electron, protons and neutrons.

protons & neutrons may be collectively referred to as nucleons

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2
Q

what are isotopes?

A

isotopes are atoms of an element that have the same proton number but different number of neutrons (& electrons)

isotopes have same chemical properties (same no. of e) but different physical properties (diff no. of n)

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3
Q

are protons deflected to the negative plate?

A

yes, protons (& cations) are deflected to the negative plate.
electrons (& anions) are deflected to the positive plate.
neutrons pass straight through

☆ if a particle is deflected to a smaller extent (smaller angle), it is because it is heavier as it has more particles. eg electrons have a much lower mass than protons so they are deflected to a greater extent. He has twice the electrons as H so He is deflected half as much as H

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4
Q

what is relative atomic mass?

A

average mass of one atom of an element ÷ (1/12 x mass of one atom of ¹²C)

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5
Q

what is relative isotopic mass?

A

mass of one atom of an isotope of an element ÷ (1/12 the mass of one atom of ¹²C)

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6
Q

what is principal quantum number?

A

principal quantum number, n, describes the main energy level of an electron. larger n = higher energy level = electron is further away from nucleus.

maximum number of electrons that can occupy each principal quantum shell is given by 2n²

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7
Q

what are the 3 rules for distributing electrons in various orbitals in an atom?

read through

A

1 - aufbau/’building up’ principle -> electrons occupy orbitals in order of energy levels; the orbital with the lowest energy is filled first (1s < 2s < 2p < 3s < 3p< 4s < 3f < 4p)
2 - hund’s rule of multiplicity -> each orbital must be singly occupied before electrons are paired
3 - an orbital cannot hold more than two electrons, and the 2 electrons sharing the same orbital must have opposite spins

group 1-2 -> s block
group 3-12 -> d block
group 13-18 -> p block (except helium which is 1s²)

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8
Q

why does atomic radius increase down the group?

A
  • down the group, no. of quantum shells increases → outermost electrons are further away from the nucleus → atomic radius increases
  • nuclear charge & shielding effect increases down the group, so effective nuclear charge differs little down the group.

no. of quantum shells is the most important factor

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9
Q

why does atomic radius decrease across a period?

A
  • across a period, number of protons increases → nuclear charge increases
  • shielding effect remains relatively constant as electrons are added to the same outermost shell
  • (nuclear charge increases while shielding effect remains relatively constant so) effective nuclear charge increasesstronger electrostatic forces of attraction between the nucleus and outermost electron
  • outermost electrons are pulled closer to the nucleus → decrease in atomic radius
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10
Q

why does atomic radius remain relatively invariant across the first row of transition elements?

A
  • no. of protons increases → nuclear charge increases
  • electrons are added to inner 3d subshell which contributes to the shielding effect
  • increasing shielding effect nullifies, to a considerable extent, the influence of each additional proton in the nucleus → effective nuclear charge remains almost constant → atomic radius is relatively invariant
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11
Q

across the same period, why does ionic radius of cations decrease, then increase from last cation to first anion, then decrease among anions?

(ionic radius across same period) (eg period3)

A
  • cations of Na, Mg, Al & Si are isoelectronic as they have the same no. of electrions (10). anions of P, S & Cl are isoelectronic as they all have 18 electrons.
  • across the 2 isoelectronic series, nuclear charge increases while shielding effect remains the same (as no. of electrons remains the same)
  • leads to increased effective nuclear charge and stronger attraction between the outermost electrons and nucleus → decreased ionic size across each series
  • there is a sharp increase in ionic radius from cationic series to anionic series as anions have one more quantum shell than cations.
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12
Q

what is first ionisation energy?

A

first ionisation energy is the energy needed to remove 1 mole of electrons from 1 mole of gaseous atoms to form 1 mole of unipositively charged atoms

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13
Q

what is the nth ionisation energy?

where n = 2, 3, 4, 5…

A

the nth ionisation energy of an element is the energy needed to remove 1 mole of electrons from 1 mole of gaseous ions with (n-1)+ charge to form 1 mole of gaseous ions wiith n+ charge

eg if there is a big increase from the 2nd to 3rd IE, it implies that the 3rd electron is in an inner quantum shell, so there are 2 electrons in the outermost or valence subshell (the atoms is grp2)

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14
Q

why does first IE decrease down a group?

A
  • down the group, no. of quantum shells increases → outermost electrons are further from the nucleus → weaker electrostatic forces of attraction between the nucleus and outermost electron → less energy is required to remove this electron
  • both nuclear charge & shielding effect increases down the group → effective nuclear charge differs little down the group (so no. of quantum shells is the more important factor)
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15
Q

why does first IE increase across period 2 & 3?

A
  • across the period, nuclear charge increases while shielding effect remains relatively the sameeffective nuclear charge increases → electrostatic forces of attraction between outermost electrons & nucleus become strongermore energy is required to remove the outermost electron → first IE increases
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16
Q

what are the 2 anomalies in trend of first IE across period 2 & 3 and why do they exist?

A

anomaly 1: small dip between Mg [1s² 2s² 2p⁶ 3s²] (grp 2) & Al [1s² 2s² 2p⁶ 3s² 3p¹] (grp 13). the 3p subshell is further away from the nucleus than the 3s subshell → weaker attraction between the nucleus & the outermost electron → less energy is required to remove the 3p electron from Al, resulting in a lower ionisation energy for Al compared to Mg

anomaly 2: small dip between P [1s² 2s² 2p⁶ 3s² 3p³] (grp 15) and S [1s² 2s² 2p⁶ 3s² 3p⁴] (grp 16). all the 3p electrons in P are unpaired. in S, 2 of the 3p electrons are paired → there is inter-electronic repulsion between the paired electrons in the 3p subshell in S → less energy than expected is required to remove one of these paired electrons from S

17
Q

why does first IE remain relatively invariant across transition elements?

A
  • first IE involves removal of a 4s electron
  • no. of protons increases → nuclear charge increases.
  • electrons are added to the 3d subshell → shielding effect increases.
  • shielding effect increases, thus nullifying, to a certain extent, the influence of each additional proton in the nucleus → effective nuclear charge remains almost constant → energy required to remove the outermost electron of each succeeding element remains relatively invariant.