S2.2: The Covalent Model Flashcards

(34 cards)

1
Q

What is the basic theory of covalent bonds?

A

Covalent bonds formed when electrons from different atoms are shared so that each atom attains a noble gas configuration

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2
Q

What is a covalent bond?

A

Electrostatic attraction between shared pairs of electrons and the positively shared nuclei on either side of the electrons

Between 2 non-metals
Electrons shared, not transferred
-> not in fixed option -> electrons in constant motion (electron clouds)
Two atomic orbitals overlap -> molecular orbital formed

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3
Q

What are the steps for drawing a Lewis structure?

A
  1. count the total number ofvalence electrons
  2. draw theskeletal structure to show how many atoms are linked to each other
  3. use a pair of crosses or dot/cross to put an electron pair in each bond between the atoms
  4. add more electron pairs to complete the octets around the atoms ( except H which has 2 electrons)
  5. if there are not enough electrons to complete the octets, form double/triple bonds
  6. check the total number of electrons in the finished structure is equal to the total number ofvalence electrons
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4
Q

What are the ‘exceptions’ to the octet rule called?

A

More then 8 electrons -> ‘expanding the octet’ rule

Less than 8 electrons -> electron deficient

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5
Q

Examples of exceptions to the octet rule

A

Incomplète octets:

H -> achieve stable arrangement by gaining an electron
-> 1s2 (helium structure)

Li -> does the same thing as helium, but lose an electron
-> 1s2, 2s1 -> 1s2

Be -> has 2 valance -> forms stable with 4 valance

B and Al -> 3 valance -> forms stable with 6

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6
Q

Multiple covalent bonds

A

Nonmetals can share more than one pair of electrons -> different types of covalent bonds

Sharing electrons -> both atoms achieve octet -> stable

-> quadruple bond not possible -> repulsion from having 8 electrons in same region between 2 nuclei too great

Double covalent bond -> two shared pairs of electrons
Triple covalent bond -> three shared pairs of electrons

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7
Q

What is bond energy?

A

Energy required to break one mole of a particular covalent bond in the gaseous state

Unit: KJ/mol

Larger bond energy = stronger covalent bond

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8
Q

What is bond length?

A

Internuclear distance of two covalently bonded atoms

Greater force of attraction between electrons and nuclei -> atoms close -> decrease bond length, increases bond strength

Number of shared pairs of electrons increase -> bond length decrease, bond strength increase
-> increased attraction

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9
Q

What is a coordinate bond?

A

Normal covalent bond -> atoms share electrons
BUT
Some atoms have lone pair of electrons that are donated to form a bond with an electron-deficient atom

Formed when both of the electrons in shared pair originate from the same atom

Shown by arrows

Ex:
carbon monoxide, hydronium ion
ammonium ion -> nitrogen donate to hydrogen

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10
Q

What is electronegativity?

A

refers to the ability of an atom to draw an electron pair towards itself in a covalent bond

defined as a relative measure of the attraction that an atom has for a shared pair of electrons when it is covalently bonded to another atom (Pauling scale used at IB)

increases across a period and up a group

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11
Q

Explain bond polarity

A

Covalent bond between two atoms of same element -> bonding pair of electrons shared equally -> non-polar bond

Bond between atoms of different elements -> bonding pair will be closer to more electronegative atom -> polar bond

Bigger the difference in electronegativity -> high the polarity

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12
Q

What does bond polarity result in?

A

Neg charge center and Positive charge center do not coincide

Electron distribution is asymmetric

Less electronegative atom has partial charge of δ+(deltapositive)

More electronegative atom has partial charge of δ-(deltanegative)
-> difference > 1.8 -> bonding pair moves completely to more electronegative atom -> ionic

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13
Q

What is the dipole moment?

A

Dipole moment -> how polar a bond is

Direction of dipole moment shown by arrow (with vertical line through end) that points to the partially negatively charged end of the dipole

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14
Q

How do you determine molecular polarity?

A

Following things in consideration:
-> polarity of each bond in the molecule
-> how the bonds are arranged in the molecule

Some molecules have polar bonds, but overall non-polar
-> polar bonds arranged such that dipole moments cancel out

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15
Q

What is VESPR theory?

A

Covalent bonds -> electrons (in outer shell) behave as a negatively charged cloud and repel each other

Minimise repulsion -> all outer shell electrons spread out as far in space as possible

Molecular shape and angles -> predicted by VALENCE SHELL ELECTRON PAIR REPULSION THOERY (VESPR theory)

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16
Q

What are the basic rules of VESPR theory?

A
  • All electron pairs and all lone pairs arrange themselves as far apart in space as is possible
  • Lone pairs repel more strongly than bonding pairs
  • Multiple bonds behave like single bonds

Used to predict shape and angle of covalent molecules/ions

17
Q

What are domains (in terms of VESPR theory)?

A

The region of negative cloud charge

Can have 1, 2, 3 pairs of electrons

18
Q

What is the order of repulsion for electron?

A

Non-bonding : non bonding > non-bonding : bonding > bonding : bonding

19
Q

Explain/draw all the molecular geometry things

A

Look at picture flashcards

20
Q

What is a covalent network structure?

A

Sometimes not possible to satisfy bonding capacity of substance in form of molecule -> covalent bonding between all adjacent atoms -> large lattice form

Basically one giant molecule

Strong covalent bonds:
High melting and boiling point
Poor conductors (exception is graphite because of delocalized electrons)

21
Q

What are some common allotropes of carbon?

A

DIAMOND:
Carbon atoms covalently bonded tetrahedrally to four other carbon
Bond angle: 109.5°
Bond length: 0.154 nm
No place of weakness -> one of hardest natural substances

GRAPHITE:
Carbon atoms covalently bonded in a trigonal planar to 3 other carbon atoms -> hexagonal layers
Bond angle: 120°
Bond length: 0.142 nm
Layers held together by weak bonds (has spare delocalized electrons)
-> distance between layers: 0.335 nm
-> atoms on same layer -> strong covalent bonds
-> between layers: intramolecular forces
-> makes it a good lubricant, conductor

GRAPHENE:
Infinite lattice of covalently bonded atoms in 2D
Single layer of carbon in repeating hexagons
1 million times thinner than paper

22
Q

What are the structure/properties of network covalent structure of silicon and silicon dioxide (silica)?

A

Si and SiO2 -> diamond like structure

Si: silicon bond covalently to four other silicon atoms tetrahedrally

SiO2: each silicon atom surrounded tetrahedrally by four oxygen -> each silicon bridged to enrichir via oxygen atom

Hard; high melting point, poor conductor
Insoluble in water and organic solvents

23
Q

What are the properties of giant covalent structures/covalent network structures?

A

High melting and boiling point:
- many and strong covalent bonds -> lots of energy required to break

Can be hard or soft:
- graphite: soft because of weak carbon layers
- diamond and silicon (IV) oxide: hard -> difficult to break SD network of strong covalent bonds

(Mostly) insoluble in water

(Mostly) poor conductors:
- main exception is graphite -> delocalized electrons in layers
- graphene too
- buckminsterfullerene (allotrope of C) -> semiconductor
- diamond and silicon (IV) dioxide do not conduct -> all four outer electrons on carbon involved in covalent bond -> no free electrons

24
Q

What are London dispersion forces?

A

A temporary attractive force that results when the electrons in two adjacent atoms occupy positions that make the atoms form temporary dipoles
-> due to uneven spread of electrons

Electrons not static -> constant motion -> any given time distribution of electrons not symmetrical

Uneven distribution -> temporary dipole
Adjacent atom’s electrons repelled by neg part of dipole + attracted to pos -> temporary INDUCED dipole

Exist in all molecules -> sometimes weak
Responsible for attractive forces between non-polar molecules
Reason why all compounds can be liquified or solidified

25
How do you number of electrons, surface area and mass affect the formation of temporary dipoles?
NUMBER OF ELECTRONS: More electrons in molecule -> greater likelihood of distortion -> greater frequency + magnitude of temporary dipoles Dispersion forces between molecules -> stronger Melting + boiling points larger SURFACE AREA: Larger the surface area of molecule -> more contact with adjacent molecules Greater ability to induce dipole in adjacent molecule -> greater LDF + higher melting/boiling points MASS: More mass -> weaker forces of attraction
26
Explain dipole-dipole forces of attractions
Polar molecules attracted to each other via electrostatic forces -> weak but stronger than LDF LDF exist in all molecules -> but some molecules permanent dipole -> molecules with permanent dipoles attract by permanent dipole-dipole bonding -> results in high boil/melt point (increased intermolecular attraction)
27
Compare butane and propanone in terms of dipole attraction
Butane and propanone -> same number of electrons Butane = no polar -> only dispersion forces Propanone = polar -> dipole-dipole and dispersion => more energy needed to break intermolecular forces between propanone molecules = propanone higher boiling point
28
Explain dipole-induced dipole attraction
Some mixture have both polar and nonpolar Permanent dipole of polar -> cause temporary separation of charge on nonpolar Acts in addition dispersion forces
29
What are van der waals forces of attraction?
A general term for all the weak forces of attraction - includes London dispersion forces - dipole-dipole forces - dipole-induced dipole forces Occur intra and inter molecularly
30
What is hydrogen bonding?
Strongest type of intermolecular force Special type of dipole-permanent dipole bonding For hydrogen bond to form need: Species with O/N/F (very electronegative) atom with an available lone pair of electrons Hydrogen attached to the O/N/F When hydrogen covalently bonded to electronegative atom -> bond very highly polarized the H becomes so δ+ charged that it can form a bond with the lone pair of an O, N or F atom in another molecule -> number of bonds depends on: Number of H atoms on O/N/F Number of lone pairs on O/N/F
31
Predicting properties of covalent molecules: meting and boiling point
When covalent molecular substance change state -> overcoming intermolecular forces Stronger forces -> more energy to break bonds -> less volatile -> higher melting/boiling point Strength of intermolecular forces increases with: Size of molecule (smaller) Polarity of molecule (more polar) Usually intermolecular forces are weaker than covalent bonds -> most covalent substances liquid or gas at room temperature
32
Predicting properties of covalent molecules: solubility
‘Like dissolves like’ -> nonpolar dissolve in nonpolar solvents —> form dispersion forces between solvent and solute -> polar dissolve in polar solvents —> form dipole-dipole interaction/H bonds between solvent and solute Covalent molecule larger -> solubility decrease -> polar part of molecule smaller part of total structure => giant covalent structure don’t dissolve -> lattice structure too great
33
Predicting properties of covalent molecules: conductivity
Covalent substance doesn’t contain any free moving charge particles -> unable to conduct electricity in solid or liquid state However in certain conditions -> some polar covalent -> ionize -> conduct Some giant covalent structure capable -> delocalized electrons
34
What is chromatography?
Technique used to separate different compounds in a mixture Substance travel by capillary action based on solubility -> substance can make more H bonds -> more attracted to stationary phase Thin layer chromatography -> inert stationary phase (eg silica) on flat unreactive surface, solvent mobile phase - silica had OH groups -> form H bonds Depending on strength of interactions with stationary phase -> separated components travel particular distance through plate -> Rf factor calculated