Atomic Structure Flashcards

1
Q

Define the atomic no.

A

No. of protons in the nucleus

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2
Q

Define the mass no.

A

Total no. of protons + neutrons in the nucleus

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3
Q

Define isotopes

A

Atoms w/ same no. protons but diff no. of neutrons

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4
Q

What decides the physical properties of an element?

A

Mass of an atom

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5
Q

What decides the chemical properties of an element?

A

No. + arrangement of e-

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6
Q

Isotopes of an element have ____ physical properties

A

Diff

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7
Q

Why do isotopes have the same chemical properties?

A

Same e- configuration

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8
Q

Who discovered the 1st model of the atom + what was it?

A
  • John Dalton
  • Described atoms as solid spheres
  • Diff. spheres made up diff. elements
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9
Q

Who discovered the 2nd model of the atom + what was it?

A
  • JJ Thomson
  • Plum pudding model
  • Discovered e-
  • Showed atoms weren’t solid + indivisible
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10
Q

Who discovered the 3rd model of the atom + what was it?

A
  • Rutherford
  • Nuclear model - tiny +ve charged nucleus surrounded by cloud of -ve e- - most empty
  • Fired +ve charged a-particles at sheet of gold instead of being deflected, most passed straight through
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11
Q

Who discovered the 4th model of the atom + what was it?

A
  • Bohr proposed e- exist in shells of fixed energy
  • When e- move btw shells, electromagnetic radiation is emitted
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12
Q

Define the relative atomic mass (Ar)

A

Average mass of an atom of an element on a scale where an atom of carbon-12 is 12

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13
Q

Define the relative isotopic mass

A

Mass of an atom of an isotope of an element on scale where an atom of carbon-12 is 12

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14
Q

Define the relative molecular mass (Mr)

A

Average mass of a molecule on a scale where an atom of carbon-12 is 12

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15
Q

Describe how an ion is formed in a TOF mass spectrometer

A
  • Electronspray ionisation - high v applied in polar solvent, gains H+ ion
  • Electron impact ionisation - fire high energy e- at sample, knocks e- off, forming +1 ion
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16
Q

What happens in the 2nd stage of mass spectrometery?

A
  • Acceleration
  • +ve charged ions accelerated by electric field
  • Same kinetic energy
  • Lighter ions move faster
17
Q

What happens in the 3rd stage of mass spectrometery?

A
  • Ion drift
  • Ions enter region w/ no electric field, just drifts
  • Lighter ions drift faster
18
Q

Explain how ions are accelerated, detected + have their abundance determined in a TOF mass spectrometer

A
  • Accelerated by attraction to +ve charged plate
  • Detected by gaining e-
  • Abundance determinded by size of current flowing in detector
19
Q

Explain how a current is formed (3)

A
  • +ve ions hit +ve metal plate
  • E- flow to +ve ion
  • Current produced
  • Current proportional to abundance
20
Q

Suggest what might cause the relative atomic of a sample to be diff from the relative atomic mass given in the periodic table (1)

A

Some isotopes absent/takes into account other isotopes

21
Q

Why is it necessary to ionise molecules when measuring their mass in TOF mass spectrometer? (2)

A
  • Only ions will interact w/ + be accelerated by electric field
  • Only ions create current when hitting detector
22
Q

Explain how TOF mass spectrometery distinguishes btw ions w/ diff masses (3)

A
  • +ve ions accelerated by electric field
  • To constant kinetic energy
  • Lighter ions move faster
  • Faster ions arrive first at detector
23
Q

Outline how to work out relative atomic mass from a mass spectrum

A
  • Multiply abundance + x axis
  • Add up total
  • Divide by total abundance
24
Q

Give the full electronic configuration of chromium

A

[Ar] 4s13d5

25
Give the full electronic configuration of copper
**[Ar] 4s13d10**
26
What happens when a transition metal become ions?
**Lose 4s** e- before 3d
27
Define the 1st ionisation energy
**Energy** needed to **remove 1 e-** from each atom in **1 mole** of **gaseous atoms** to **form 1 mole** of **gaseous 1+ ions**
28
What is the equation for the 1st ionisation energy?
**x (g) → x+ (g) + e-**
29
What are the factors affecting ionisation energy?
* **Nuclear charge** - **more protons** = **stronger FOA** * **Distance from nucleaus** - **closer** * **Shielding** - **less e-**
30
Define high ionisation energy
**High attraction** btw **e-** + **nucleus** so **more energy needed** to **remove e-**
31
Define the 2nd ionisation energy
**Energy needed** to **remove 1 e-** from each **ion** in **1 mole** of **gaseous 1+ ions** to **form 1 mole** of **gaseous 2+ ions**
32
What is the equation for the 2nd ionisation energy?
**x(n-1)+ (g) → xn+ (g) + e-**
33
Explain why the 2nd ionisation energy is higher than the 1st ionisation energy?
* **More energy needed** to **remove e-** from **more +ve ion** * **Less repulsion** * **Stronger FOA**
34
Explain the ionisation energy trend in group 2
* **Dec** * **Atom radius inc** * **More sheilding**
35
Explain the general trend in ionisation energy across period 3
* **Inc** * **More protons** * **Same shielding** * **Stronger FOA** for **outer e-**
36
Explain why a deviation occurs btw group 2 + 3 first ionisation energy in period 3 (3)
* **Al lower** than **Mg** * **Outer e-** in **3p orbital** * 3p is **higher** in **energy**
37
Explain why a deviation occurs btw group 5 + 6 first ionisation energy in period 3 (3)
* **S lower** than **P** * **Outer e-** in **3p orbital** begin to **pair** * **Electron pair repulsion**