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50 Cards in this Set
- Front
- Back
Octet rule |
Atoms TEND to lose, gain, or share electrons till they are surrounded by eight valence elctrons |
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Characteristics of Noble gases ( 3) |
1) High I.E 2) Low affinity for additional electrons 3) General lack of reativity |
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Define ionic bond |
Electrostatic force of attraction between 2 oppositely charged ions ( Between metals and non-metals) |
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Covalent Bond |
The attraction between the localised shared electrons and the nuclei (between non-metals) |
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Define dative bond |
Shared pair of electrons is provided by only one of the bonding atoms |
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Conditions for co-ordinate bond (2) |
1) Lone pair of electrons for the donor 2) Vacant low-lying orbital for the acceptor |
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Relationship between cat/anions and electronegativity |
For cations (e.g. NH4+) electrons are lost from the less electronegative atom (usually central atom) For anions (e.g. S04 2- ) electrons are gained by the more electronegative ion |
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Less than 8 electrons in valence shell = ? |
Electron deficient |
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Molecules with unpaired electrons (e.g. n02) = ? |
Radicals |
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Why can Pcl5 exist but not Ncl5? |
Expansion of octet is only available for elements in period 3 or more , as they will have the low-lying vacant orbitals to accommodate the expansion. N is from period 2 . |
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What is the VSEPR Theory and what is it used for |
Valence Shell Electron Pair repulsion Theory To predict the molecular geometry or shape of a species |
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2 Principles of the VSEPR Theory |
1) Electron pairs around the central atom of a molecule are arranged as far apart as possible to minimise inter-electronic repulsion - to have the greatest stability 2) Lp - lp repulsion > bp-lp repulsion > bp-bp repulsion |
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Is a double bond 2 regions of electron density? |
NO |
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2 regions of electron density |
0 lp - Linear - 180 |
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3 regions of electron density |
0lp - trigonal planar - 120 1lp - bent - <120 |
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4 regions of electron density |
0lp - tetrahedral - 109.5 / 109 1lp - trigonal bypyramidal - 107 2lp - bent - 105 |
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5 regions of electron density |
0lp - Trigonal bipyramidal - 120 + 90 1lp - Seesaw - NA 2lp - T-Shape - 90 3lp - Linear - 180 |
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6 regions of electron density |
0lp - Octahedral - 90 1lp - square pyramidal - NA 2lp - Square planar - 90 |
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Effect of electronegativity of central atom on bond angles |
More electronegative - draws electron density to itself - bond pair is nearer to the nucleus - exert more repulsion |
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Covalent bonding is the overlapping of valence orbitals - why does the overlapping need to be effective ? |
To ensure that the electron density in the region between the nuclei is a maximum |
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What is the condition for the optimum bonding distance? |
Molecule must be most stable - when the energy level is at a minimum |
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Two types of Covalent bond depending on the way the orbital overlap |
1) Sigma bond 2) pi bond |
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Characteristics of sigma bonds 1) Type of overlap 2) Type of orbitals 3) Electron density concentration |
1) Head to head overlap of 2 atomic orbitals 2) Can be s,p, or d orbitals 3) Electron density is concentrated between the nuclei of the two bonding atoms |
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Characteristics of pi bonds 1) Type of overlap 2) Type of orbitals 3) Electron density concentration |
1) Collateral , side-on overlap 2) p or d orbitals 3) Electron cloud above an below the nuclear axis but 0 electron density along the axis |
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Comparison between the two types |
1) pi bond is weaker as the side - on overlap is less effective |
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Can pi bonds exist in single bonds ? |
No. pi bonds occur when atoms undergo multiple bonding - one of the bonds must be a sigma bond, and the rest are pi bonds E.g. triple bond consists of one sigma and 2 pi bonds |
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Relationship between covalent bond length and strength of covalent bond |
Stronger the covalent bond - shorter the bond length |
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Bond energy = bond enthalpy ? |
YEP |
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Define bond energy |
The average energy absorbed when 1 mol of a particular bond is broken in the gaseous state |
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Factors affecting covalent bond strength (3) |
1) Number of bonds between atoms 2) Effectiveness of overlap between orbitals 3) Difference in electronegativities of the bonding atoms (bond polarity) |
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1) Number of bonds between atoms |
Increased number of bonds - increased number of shared electrons btw the 2 atoms - increased electrostatic attraction btw bond pairs and nuclei - bond strength increases |
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2) Effectiveness of overlap of the orbitals |
Larger orbitals - more diffuse - overlap is less effective |
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3) Difference in electronegativities in the bonding atoms |
Different electronegativities - electron density distribution is asymmetrical - partial charges arise on the bonded atoms - polar covalent bond - increase in electrostatic attraction ( between delta + and data - ) - increased bond strength Simply put : Greater the difference in electronegativities - higher the bond parity - stronger the bond |
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What is hybridisation? |
Term applied to the mixing of atomic orbitals in an atom to generate a set of hybrid orbitals |
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What does sp3 hybridisation lead to ? |
tetrahedral electron pair geometry |
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What does sp2 hybridisation lead to ? |
Trigonal planar electron pair geometry |
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What does sp hybridisation lead to |
linear electron pair geometry |
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What about the unhybridized orbitals? |
They remain ; perpendicular to each other and the line containing the hybridised orbital |
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Effect of hybridisation one bond strength and length |
Since s orbital is spherical and closer to the nucleus , the higher the s character of the hybrid orbital - more effective overlap with orbital of other atoms - increase in bond strength and decrease in bond length E.g. sp has more s character than sp3 |
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What is in a resonance hybrid(e.g. O3) |
pi bonding electrons are delocalised over the atoms via the overlapping of p orbitals of atoms , which are perpendicular to the plane of the molecule ( containing sigma bonds) |
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Why resonance hybrid? |
More stable than any of the other resonance structures |
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Range of bond types |
Ionic - Ionic with partial covalent character - polar covalent bond - non polar / pure covalent bond |
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Formation of ionic bonds with covalent character |
Attraction of the cation for the valence shell electrons of the anion - distortion / polarisation of the electron cloud - pulling it into the region between the two nuclei - electron sharing , ergo, covalency |
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Degree of covalent character depends on (2) |
1) Polarising power of the cation - in turn dependent on the charge density 2) Polarisability of the anion depends on the size of the anion and charge |
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Formation of Polar covalent bond |
Two atoms with different electronegativities - electron pair is not equally shares - bond becomes polar |
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Degree of polarity depends on |
Dipole moment - Dependent on difference in electronegativities. The product of the charge of the distance between the charges Indicated by an arrow with a line striking close to the end |
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What is the overall dipole moment of a molecule ? |
The vector sum of all the bond dipol moments |
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Is Co2 a polar molecule ? |
No. Although the CO bonds are polar covalent bonds, the bond dipole moments cancel each other out vectorially - overall dipole moment is 0 |
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Which molecular shapes cancel out the bond dipole moments of polar covalent bonds? |
Linear , trigonal planar, tetrahedral, trigonal bipyramidal, octahedral * all shapes without any lone pairs |
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C-H bond ; is it polar? |
No . the electronegativity difference is almost zero - thus it is negligible |