Group IA Alkali Metals & Their Compounds

electron structure

one electron in outer shell

found in group 1

similar physical and chemical properties

readily lose the outer shell electron to form positive ions with a +1 charge

trend in density

down the group, more dense but the trend is not perfect because K is less dense than Na.

properties

physical properties

• Soft metals with silvery colour.

• Good thermal/electrical conductors

• Li -> K - less dense than water,

• Rb&Cs –more dense

• Kept in oil in order to avoid oxidation

• Melting points decreases down the group

• Ionic/atomic radii increases down the group

• Density increases down the group

• Ionization energy,IE decreases down the group

• Electron affinity, EA decreases down the group (magnitude)

•Adhering properties increased down the group

general

Each atom in this group consist of one valence
electron in the s orbital

reactivity of metal

down a group

  • Increase in size
  • Increase in shielding effect
  • Decrease in Ionization Energy (IE) - Low ionization energy

exist as ionic compunds
eg: NaCl

compounds

Lattice energy of the salt

Hydration energy

The separation of free ions in gas phaseneed energy so /_\Hlatt (+ve)
M+X-(s) -> M+(g) + X-(g)

crystal structure: Body Centered Cubic (BCC)

exist as covalent compounds
eg: Na2

soluble in water

normally white in colour except KMnO4-purple

very high melting points

towards free ions involves released energy -> Esolv./hyd (-ve)
M+(g) + X-(g) -> M+(aq) + X-(aq)

colour of flame

Li- crimson
Na- yellow
K- red- lilac/violet
Rb- red
Cs- blue

the smaller the size of the ions, the bigger the ionic charge -> the stronger the bond between ions and solvent. So, more energy is released.

solubility

Hydration energy

the smaller the size of the ions, the bigger the ionic charge -> the stronger the bond between ions and solvent. So, more energy is released.

towards free ions involves released energy -> Esolv./hyd (-ve)
M+(g) + X-(g) -> M+(aq) + X-(aq)

Lattice energy of the salt

The separation of free ions in gas phase

  • need energy so /_\Hlatt (+ve)
    M+X-(s) -> M+(g) + X-(g)

ion size: Li+ < Na+ < K+ < Rb+ < Cs

existence

Li

Petalite

Ambligonite

Spodumene

Na

Rock salt

Sea water

Chile saltpeter in Chile

Soda lakes

Borax, at Nevada USA

Cryolite

K

Silvin

Carnalite

Kainite

Leonite

extraction

K, Rb and Cs Metals

K cannot be obtained by electrolysis of the KCl due to

  • the melting point of KCl (776 °C) is higher than K metal (762 °C)
  • K metal dissolves in molten salt
  • Discharge potential for K+ and Ca2+ is similar, if the molten used KCl-CaCl2

Reduction of molten chloride with Na vapour
MCl(l) + Na(g) M(l) + NaCl(l) e.g. Potassium
KCl(l) + Na(g) NaCl(s) + K(l)

application

Lithium

LiAlH4 - reducing agents for organic compounds – produce H.

Lithium complex oxide, LiNbO3 – use in mobile communication devices – due to nonlinear optical and acousto-optical effect

sodium

as coolant in reactor nuclear

NaCl – flavouring food, road de-icing

Potassium

Cs – alloy with Al and Ba is used in photoelectric cell

chemical

wet air
(O2, H2O, CO2)

  • Slow to form oxide -> hydroxide -> carbonate

4M + O2 -> 2M2O (M= Na, K)

M2O + H2O -> 2MOH

2MOH + CO2 + nH2O -> M2CO3.nH2O

H20

Very reactive H2 evolve, base solution

M+2H2O->2MOH+ H2 (M=Li < Na < K < Rb <.Cs)
increasing alkalinity

compounds of alkali metals

metal is extremely reactive

  • Very Electropositive, forming positive ions
    (Cations) -> act as Electron Donor

hydrides

oxides

monoxide (M2O)

peroxide (M2O2)

superoxide (MO2)

carbonates (M2CO3)

nitrate

preparation

physical properties

  1. Directly from metal and H2 gas->form saline hydride
  2. Reaction between group IA oxides in a flow of H2 gas
    M2O(s) + H2(g) -> MH(s) + MOH(s)

ionic crystal

colourless

m/p: LiH=700oC, NaH/KH~400oC

reactions

React violently with water

Reaction with alcohol -> alcoholate

Reaction with liquid ammonia -> amide

Reaction with oxygen -> oxide

uses

As reducing agent : produce H2

as source of hydrogen gas

as fuel

uses

as bleaching agent

to get rid of CO2 and produce O2 in a closed area

hydroxide

NaOH & KOH:
Industrial Process

electrolysis

  • Electrolyte: Brine (Concentrated NaCl)
  • Anode: Carbon (Graphite),
  • Cathode : Mercury

uses

soap industry

bleaching agent

Solvay process

Na2CO3

properties

Colourless and transparent solid


Exist as hydrated salt

application

A precursor for GLASS manufacturing industries

In manufacture of sodium silicate/water glass

Manufacturing of soap and detergent

As hard water softener

Manufacturing of borax

K2CO3

MHCO3

Application

NaHCO3

baking powder

fire extinguisher

KHCO3

gastric medicine

buffer in wine product & water treatment

buffer in low pH liquid detergent

NaNO3

KNO3

• Deliquescent solid
• Used in making other nitrates, fertilizers and explosives

  • Naturally occurs as mineral saltpetre
  • Slightly soluble in cold water but very soluble in hot water
  • Used in manufacturing explosives, fireworks, matches and fertilizers

halides (MX)

Trend of /\Hf
• F- to I- : /
\ Hf becomes less negative due to increase radius of the anion and , /_\Hlatt becomes less negative

down the group,

  • /_\Hf for Cl-, Br-, I- becomes
    more negative
  • /\Hf for F- becomes less negative due to increase in radius of M+ , /\Hlatt also
    decrease (less negative)

Thermal & Solubility of Salt of Group IA

stable- high electro+ve charge

Li2CO3 – decompose upon heating
Li2CO3->Li2O + CO2
Other carbonate : do not decompose

Anomaly of Lithium from other alkali metals

Exhibit covalent character in its bonding

Form normal oxide, Li2O

LiH is stable to heating to 900oC, Other hydride decompose above 400oC

Diagonal Relationship (Li-Mg)

due to similar in atomic size and electronegativity,

Only form low oxide (normal) when heated in oxygen/air

carbonates easily decomposed to CO2 and an oxide when heated.

sulphates and carbonates salts insoluble in water

Formed carbides and nitrides on direct heating in C and N2

Halides soluble in various organic solvents

nitrates decomposed to an oxide, nitrogen dioxide and oxygen
when heated