2. Atoms, molecules and stoichiometry Flashcards

1
Q

define the unified atomic mass unit

A

one twelfth of the mass of a carbon-12 atom

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2
Q

define relative atomic mass, Ar, relative isotopic mass, relative molecular mass, Mr, and relative formula
mass in terms of the unified atomic mass unit

A

Ar-

Mr-

isotopic mass-

relative formula mass-

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3
Q

define and use the term mole in terms of the Avogadro constant

A
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4
Q

common ions

A

NO3–, CO32–, SO42–, OH–, NH4+, Zn2+, Ag+,HCO3–, PO4 3–

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5
Q

define and use the terms empirical and molecular formula

A

empirical-

molecular-

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6
Q

understand and use the terms anhydrous, hydrated and water of crystallisation

A
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7
Q

perform calculations including use of the mole concept, involving:

(a) reacting masses (from formulas and equations) including percentage yield calculations

(b) volumes of gases (e.g. in the burning of hydrocarbons)

(c) volumes and concentrations of solutions

(d) limiting reagent and excess reagent

A

moles= mass/ Ar/Mr
moles= volume*conc
moles= volume/24

% yield= actual yield/theoretical yield

% composition=mass/total mass*100

limiting-excess= ratio of moles and lower moles is limiting.

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8
Q

define electronegativity

A

power of an atom to attract electrons to itself

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9
Q

explain the factors influencing the electronegativities of the elements

A

nuclear charge-
atomic radius-
shielding by inner shells and sub-shells-

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9
Q

explain the trends in electronegativity across a period and down a group

A
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10
Q

use the differences in Pauling electronegativity values to predict the formation of ionic and covalent bonds

A

< 1- covalent
1-2 - polar covalent
> 2-ionic

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11
Q

ionic bonding with examples

A

electrostatic attraction between oppositely charged ions (positively charged
cations and negatively charged anions)

sodium chloride, magnesium oxide and calcium fluoride

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12
Q

define metallic bonding

define covalent bonding

A

electrostatic attraction between positive metal ions and delocalised electrons.

electrostatic attraction between the nuclei of two atoms and a shared pair of
electrons.

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13
Q

describe covalent bonding in molecules including:
* hydrogen, H2
* oxygen, O2
* nitrogen, N2
* chlorine, Cl 2
* hydrogen chloride, HCl
* carbon dioxide, CO2
* ammonia, NH3
* methane, CH4
* ethane, C2H6
* ethene, C2H4

A
  • hydrogen, H2- 1 pair
  • oxygen, O2- 2 pairs
  • nitrogen, N2- 3 pairs
  • chlorine, Cl 2- 1 pair
  • hydrogen chloride, HCl- 1 p
  • carbon dioxide, CO2- 2-2 p
  • ammonia, NH3- 1,1,1
  • methane, CH4- 1,1,1,1
  • ethane, C2H6 1 bw all
  • ethene, C2H4 2 bw C, 1 bw C-H
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14
Q

period 3 property of octet

A

period 3 can expand their octet including in the compounds sulfur dioxide, SO2, phosphorus pentachloride, PCl 5 , and sulfur hexafluoride, SF6

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15
Q

describe coordinate (dative covalent) bonding

A

reaction between ammonia and hydrogen chloride gases to form the ammonium ion, NH4+, and in the Al 2Cl 6 molecule

16
Q

describe covalent bonds in terms of orbital overlap giving σ and π bonds:

A
  • σ bonds are formed by direct overlap of orbitals between the bonding atoms
  • π bonds are formed by the sideways overlap of adjacent p orbitals above and below the σ bond
17
Q

use the concept of hybridisation to describe sp, sp² and sp³ orbitals

17
Q

describe how the σ and π bonds form in molecules including H₂, C₂H₆, C₂H₄, HCN and N₂

18
Q

define bond energy and bond length.

use bond energy values and the concept of bond length to compare the reactivity of covalent molecules

A

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

the internuclear distance of two covalently bonded atoms

19
Q

state and explain the shapes of, and bond angles in, molecules by using VSEPR theory, including as
simple examples:

A
  • BF3 (trigonal planar, 120°)
  • CO2 (linear, 180°)
  • CH4 (tetrahedral, 109.5°)
  • NH3 (pyramidal, 107°)
  • H2O (non-linear, 104.5°)
  • SF6 (octahedral, 90°)
  • PF5 (trigonal bipyramidal, 120° and 90°)

trigonal planar- 3B 0L
linear- 2B, 0L
tetrahedral- 4B, 0L
pyramidal- 3B, 1L
non-linear- 2B, 2L
trigonal bipyramidal- 5B, 0L
octahedral- 6B, 0L

20
Q

describe hydrogen bonding

A

molecules containing N–H and O–H groups.
ammonia and water- examples

21
Q

use the concept of hydrogen bonding to explain the anomalous properties of H₂O

A
  • its relatively high melting and boiling points
  • its relatively high surface tension
  • the density of the solid ice compared with the liquid water
22
Q

use the concept of electronegativity to explain bond polarity and dipole moments of molecules

23
Q

describe van der Waals’ forces- generic term to describe all intermolecular forces.

describe the types of van der Waals’ forces:

A

the intermolecular forces between molecular entities other than those due to bond formation.

  • instantaneous dipole–induced dipole (id-id) forces, also called London dispersion forces
  • permanent dipole–permanent dipole (pd-pd) forces, including hydrogen bonding
24
Q

describe hydrogen bonding and state order of strength of bonds

A

hydrogen bonding is a special case of permanent dipole–permanent dipole forces between molecules where hydrogen is bonded to a
highly electronegative atom. FONCl.

in general, ionic, covalent and metallic bonding are stronger than intermolecular forces.