bonding Flashcards

(48 cards)

1
Q

ionic bonding def

A

the electrostatic force of attraction between oppositely charged ions

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2
Q

when is ionic bonding stronger and the mp higher

A

when the ions are smaller and have higher charges

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3
Q

why are positive ions smaller

A

it has one less shell of electrons;
ratio of protons to electrons has increased so there is a stronger attraction to hold the remaining electrons

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4
Q

why are negative ions bigger

A

negative ions have more electrons than the element, but the same number of protons;
the attraction from the nucleus is shared over more electrons, making it weaker and the ions bigger

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5
Q

trend in ionic radii down a group

A

size of ionic radii increases;
as you go down the ions have more shells

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6
Q

covalent bond

A

the electrostatic force of attraction between the nuclei and bonding pair of electrons

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7
Q

dative/coordinate covalent bond

A

when the shared pair of electrons come from only one of the bonding atoms
e.g. NH4+, H3O+

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8
Q

metallic bonding

A

the electrostatic force of attraction between rhetorical positive metal ions and the delocalised electrons

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9
Q

factors that affect the strength of metallic bonds

A
  1. number of protons/strength of nuclear charge (more positive=stronger bond)
  2. number of delocalised electrons (more delocalised electrons=stronger bond)
  3. size (smaller ion=stronger bond)
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10
Q

why does Mg have stronger metallic bonding than Na

A

the metallic bonding gets stronger because Mg has more electrons that become delocalised;
Mg ion is smaller and has one more proton so a higher nuclear charge;
stronger electrostatic force of attraction between the positive metal ions and the delocalised and more energy is needed to break bonds

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11
Q

structure of compounds w ionic bonds

A

giant ionic lattice
e.g. sodium chloride (NaCl), magnesium oxide (MgO)

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12
Q

structure of compounds w weak covalent bonds

A

simple molecular;
vdw, permanent dipoles, H bonds between molecules
e.g. iodine, CO2, H2O, CH4

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13
Q

structure of compounds w strong covalent bonds

A

macromolecular;
e.g. diamond, graphite, silicon dioxide, silicon

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14
Q

structure of compounds w metallic bonds

A

giant metallic lattice
e.g. magnesium, sodium, all metals

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15
Q

melting and boiling points of ionic compounds/lattices

A

high;
because of giant lattice of ions with strong electrostatic forces between oppositely charged ions

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16
Q

solubility in water of ionic compounds

A

generally good

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17
Q

conductivity of ionic compounds when solid

A

poor; ions can’t move / fixed in place

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18
Q

conductivity of ionic compounds when molten

A

good; ions can move

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19
Q

melting and boiling points of simple molecular molecules

A

low; because of weak IM forces between molecules

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20
Q

solubility in water of simple molecular compounds

A

generally poor

21
Q

conductivity of simple molecular molecules when solid

A

poor; no ions to conduct and electrons are fixed in place

22
Q

conductivity of simple molecular molecules when molten

A

poor; no ions

23
Q

melting and boiling points of macromolecular substances

A

high;
because of many strong covalent bonds in macromolecular structure;
takes a lot of energy to break the strong bonds

24
Q

solubility in water of macromolecular substances

25
conductivity of macromolecular substances when solid
diamond and sand: poor; because electrons can’t move (localised); graphite: good; as free delocalised electrons between layers
26
conductivity of macromolecular substances when molten
poor
27
melting and boiling points of metallic structures
high; strong electrostatic forces between positive ions and delocalised sea of electrons
28
solubility in water of metallic structures
insoluble
29
conductivity of molten substances when solid
good; delocalised electrons can move through structure
30
conductivity of metallic structures of molten
good
31
linear molecules
2 bonding pairs, no lone pairs, 180° e.g. CO2, CS2, HCN, BeF2
32
trigonal planar
3 bonding pairs, no lone pairs, 120° e.g. BF3, AlCl3, SO3
33
tetrahedral molecules
4 bonding pairs, no lone pairs, 109.5° e.g. SiCl4, SO4^2-, ClO4^-, NH4^+
34
trigonal pyramidal molecules
3 bonding pairs, 1 lone pair, 107° e.g. NCl3, PF3, ClO3, H3O^+
35
bent molecules
2 bonding pairs, 2 lone pairs, 104.5° e.g. OCl2, H2S, OF2, SCl2
36
trigonal bipyramidal
5 bonding pairs, no lone pairs, 120° and 90° e.g. PCl5
37
octahedral
6 bonding pairs, no lone pairs, 90° e.g. SF6
38
electronegativity
the ability for an element to attract a lone pair of electrons in a covalent bond
39
factors affecting electronegativity
electronegativity increases as: nuclear charge increases and atomic radii decreases because electrons are pulled in more so there’s a stronger attraction
40
why does electronegativity decrease down the group
the distance between the nucleus and the outer electrons increases and the shielding of inner shell electrons increases
41
formation of a permanent dipole
a polar covalent bond forms when the elements in the bond have different electronegativities; when a bond is polar, it has an unequal distribution of electrons and produces a charge separation
42
symmetric molecule
all bonds identical; no lone pairs; not polar even if individual bonds within the molecule are polar e.g. CO2
43
van der waals
occurs between all molecular substances and noble gases; not in ionic substances
44
factor affecting size of vdw
the more electrons there are, the higher the chance that temporary dipoles will form, this makes the vdw stronger between molecules so bp will be greater
45
explain the reason for increasing boiling points down group 7
increasing number of electrons, causing an increase in the size in vdw; iodine is solid and chlorine is a gas
46
why do longer chain alkanes have stronger vdw
have a larger SA of contact between molecules for vdw to form than spherical shaped and branched alkanes, so stronger vdw
47
permanent dipole
occurs between polar molecules; stronger than vdw so have higher bp; commonly compounds with C-Cl, C-F, C-Br, H-Cl, C=O; asymmetrical and have a bond where there’s a significant difference in electronegativity
48
hydrogen bonding
when H is attached to the 3 most electronegative elements; F, O, N strongest IM force