bonding alevel chemistry

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45 Terms

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ionic bonding

electrostatic force of attraction between oppositely charged ions formed by electron transfer.

<p>electrostatic force of attraction between oppositely charged ions formed by electron transfer.</p>
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how can ionic bonds be stronger

stronger and the melting points higher when the ions are smaller and/ or have higher charges

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giant ionic lattice and ionic bonds reaction in water

-regular structure -cubic shape -giant repeating pattern -most ionic compounds dissolve in water as water is polar -attracts the + and - charges break up structure

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ionic bonds conduct electricity and have high melting points because?

-molten or dissolved as ions are free to move around -there are many electrostatic forces between ions -lots of energy to overcome these forces

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Covalent bonding

sharing of outer electrons to form a full outer shell -electrostatic attraction between nucleus and shared electrons

<p>sharing of outer electrons to form a full outer shell -electrostatic attraction between nucleus and shared electrons</p>
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electrons in covalent bonds

pair to form multiple covalent bonds

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dative covalent bonds

the shared pair of electrons in the covalent bond come from only one of the bonding atoms. A dative covalent bond is also called co-ordinate bonding.

<p>the shared pair of electrons in the covalent bond come from only one of the bonding atoms. A dative covalent bond is also called co-ordinate bonding.</p>
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metallic bonding

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

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the factors affecting metallic bonding

-Number of protons/ Strength of nuclear attraction. -Number of delocalised electrons per atom -Size of ion

<p>-Number of protons/ Strength of nuclear attraction. -Number of delocalised electrons per atom -Size of ion</p>
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there are 4 types of crystal structure

ionic, metallic, simple molecular, macromolecular

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molecular properties

low bp because of weak intermolecular forces between molecules -poor solubility -poor conductivity no ions -mostly liquids and gases -electrons localised

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macromolecular properties

-high melting points -many strong covalent bonds in macromolecular structure -lot of energy to break many strong bonds -insoluble -conductivity poor (not graphite) -poor when molten -solids

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metallic bonding properties

-high mp/bp strong electrostatic forces between + ions and negative sea electrons -good conductivity -delocalised electrons and molten

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description of metallic bonding

shiny metal -Malleable as the positive ions in lattice are all identical -planes of ions can slide easily over one another -attractive forces in the lattice are same whichever ions are adjacent

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Shapes of molecules

-bond pairs and lone pairs -specific shape specific angles -bond pairs repel each other equally -electrons repel -lone pair repel bonding pairs more as they are attracted to same nucleus -2.5 degrees -and repel bonding bonding pairs

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rules shapes of molecules

maximum repulsion -minimum separation

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Lone pair repulsion

-lone pairs around central atom provides additional repulsive forces, because the lone pair closer to nucleus of atom, while bp is attracted to other nucleus
-for every lone pair there is a reduction of 2.5 degrees

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Molecule shape

-linear -trigonal planar -tetrahedral -trigonal pyramidal -bent -trigonal bipyramidal -octahedral

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Tetrahedral

109.5 bp: 4

<p>109.5 bp: 4</p>
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trigonal pyramidal

3 bonds, 1 lone pair, 107 bond angle

<p>3 bonds, 1 lone pair, 107 bond angle</p>
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trigonal bipyramidal

90-120 bp: 5

<p>90-120 bp: 5</p>
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octahedral

bp: 6 90 degrees

<p>bp: 6 90 degrees</p>
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Linear

BP: 2 LP: 0 ANGLE: 180

<p>BP: 2 LP: 0 ANGLE: 180</p>
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V-shaped (bent)

BP:2 LP:2 ANGLE:104.5

<p>BP:2 LP:2 ANGLE:104.5</p>
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Trigonal planar

BP:3 LP: 0 120

<p>BP:3 LP: 0 120</p>
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Electronegativity

tendency of an atom in a covalent bond in a molecule to attract electrons in a covalent bond to itself.

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how is it measured

Electronegativity is measured on the Paulings scale(ranges from 0 to 4) F, O, N, CL are the most electronegative -most en is fluorine

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how is electronegativity affected?

-increases across a period as the number of protons increases and the atomic radius decreases because the electrons in the same shells
-distance between the nucleus and the outer electrons increases and the shielding of inner shell electrons increases

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intermediate bonding

Ionic and covalent bonding are the extremes of a continuum of bonding type. Differences in electronegativity between elements can determine where a compound lies on this scale

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elements of similar electronegativity and hence a small electronegativity difference will be

will be purely covalent

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elements in a compound with a large electronegativity difference

>1.7 ionic

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polar covalent bond

-different electronegativities -unequal distribution of electrons -produces charge separation -dipole -unsymmetric

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symmetric molecules

non-polar as dipoles cancel out -not net dipole moment

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vaan der waals occur in

-all molecular substances and noble gases-do not occur in ionic substances -transient, induced dipole-dipole interactions -occur between all simple covalent molecules and the separate atoms in noble gases

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van der Waals forces

a slight attraction that develops between the oppositely charged regions of nearby molecules

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Why do van der Waals interactions occur?

electrons are moving constantly, randomly -electron density can fluctuate -parts of the molecule become more or less negative i.e. small temporary or transient dipoles form.

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factors affecting van der waals?

-more electrons there are in the molecule the higher the chance that temporary dipoles will form. -Van der Waals stronger between the molecules and so boiling points will be greater

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Van der waal in branched vs straight chained alkanes

-Long chain alkanes -larger surface area of contact between molecules -Van der Waals to form than compared to spherical shaped branched alkanes and so have stronger Van der Waals

<p>-Long chain alkanes -larger surface area of contact between molecules -Van der Waals to form than compared to spherical shaped branched alkanes and so have stronger Van der Waals</p>
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Permanent dipole-dipole force

between polar molecules -stronger than Van der Waals and so the compounds have higher boiling points -Polar molecules have a permanent dipole

<p>between polar molecules -stronger than Van der Waals and so the compounds have higher boiling points -Polar molecules have a permanent dipole</p>
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polar molecules are

asymmetrical and have a bond where there is a significant difference in electronegativity between the atoms -permanent dipoles have electrostatic forces between them

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hydrogen bonding

hydrogen atom attached to one of the three most electronegative atoms of nitrogen, oxygen and fluorine -an available lone pair of electrons -large electronegativity difference between the H and the O,N,F

<p>hydrogen atom attached to one of the three most electronegative atoms of nitrogen, oxygen and fluorine -an available lone pair of electrons -large electronegativity difference between the H and the O,N,F</p>
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all intermolecular forces must

have van der waals as well

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ice

-forms a regular structure -held by hydrogen bonding -molecules further apart -less dense then water

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graphite (macromolecule giant covalent)

-pencil lead -layers slide easily (weak forces) -delocalised electrons -conduct electricity -low density -layers are far apart -insoluble high mp -covalent bonds

<p>-pencil lead -layers slide easily (weak forces) -delocalised electrons -conduct electricity -low density -layers are far apart -insoluble high mp -covalent bonds</p>
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diamond

-tightly packed rigid arrangement -allows heat to conduct well -doesn't conduct electricity -insoluble and high mp because of covalent bonds -gemstones -no delocalized electrons

<p>-tightly packed rigid arrangement -allows heat to conduct well -doesn't conduct electricity -insoluble and high mp because of covalent bonds -gemstones -no delocalized electrons</p>