the group 1a and group 2a elements.pdf

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Cotton chapter  10,11

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Cotton chapter

 10,11

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Group 1A

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Group 1A

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Qualitative alkali

 metal

 analysis

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Alkali Metals

 The group 1A elements with their ns1  valence electron

configurations are very active metals. They lose their valence electrons very readily. They have low ionizationenergies and react with nonmetals to form ionic solids.

2Na(s) + Cl2(g) 2NaCl(s)  The expected trend in reducing ability,

Cs>Rb>K>Na>Li

 Alkali metals all react vigorously with water to releasehydrogen gas.

2M(s) + 2H2O(l) 2M+(aq) + 2OH‐

(aq) + H2(g)

 Observed reducing abilities: Li>K>Na

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First ionization

 energy

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Soda production

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Properties and

 Trends

 in

 Group

 1A

 The Group 1A  metals exhibit regular  trends for a 

number of  properties. Irregular  trends suggest that factors are  working 

against each other in determining a property  (such as 

the density  “discrepancy” between sodium and potassium).

 The alkali metals have two notable physical properties: 

they  are all soft and have low melting points. When freshly  cut, the alkali metals are bright and 

shiny—typical metallic properties. The metals quickly  

tarnish, however,

 as

 they 

 react

  with

 oxygen

 in

 the

 air.

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Alkali Metal

 Oxides

In the presence of ample oxygen,

4Li + O2   →   2Li2O (regular oxide)

2Na + O2   →   Na2O2 (peroxide)K + O2   →   KO2 (superoxide)

Rb + O2   →   RbO2 (superoxide)

Cs + O2   →   CsO2 (superoxide)

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The oxides

 of 

 Group

 1A

Direct reaction of  the alkali metals  with O2 gives :Li  ‐> oxide, peroxide (trace)Na  ‐> peroxide , oxide (trace)

K,Rb,Cs  ‐> superoxide

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Diagonal Relationships:

The Special

 Case

 of 

 Lithium

In some of  its properties, lithium and its compounds 

resemble magnesium and its compounds.   Lithium carbonate, fluoride, hydroxide, and phosphate are 

much less  water soluble than those of  other alkali metals.

  Lithium is the only  alkali metal that forms a nitride (Li3N).

  When it burns in air, lithium forms a normal oxide (Li2O) 

rather than a peroxide or a superoxide.

  Lithium carbonate and lithium hydroxide decompose to form 

the oxide on heating,  while the carbonates and hydroxides of  other Group 1A  metals are thermally  stable.

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Diagonal

Relationships

The 

elements 

in 

each encircled pair have

several similar properties.

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Occurrence, Preparation, Use, and 

Reactions of 

 the

 Alkali

 Metals

 Sodium and potassium are isolated primarily  from 

brines 

(solutions of  NaCl and KCl). Lithium is obtained mostly  from the mineralspodumene, LiAl(SiO3)2.

 To convert an alkali metal ion into an alkali metal atom, the ion must take on an electron—a process of  reduction.

 This is not easy   with the alkali metals; they  are excellent reducing agents.

 Potassium  was the first alkali metal to be prepared by  

electrolysis.

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The Hydroxides

 of 

 Group

 1A

 The hydroxides are  white crystalline solids

 NaOH (318  C̊)

 KOH  (360  C̊)

 Hydroxides are freely  soluble exothermically  in  water and in alcohols

 Strong alkali bases

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Ionic salts

 Li has some special properties as compared to the 

other elements of  group 1

 LiOH is less soluble then the other Hydroxides

 Li3N is

 stable

 (the

 only 

 stable

 Nitrite

 in

 this

 group)

 Electrical conductive

 Precipitation reactions: The larger the M‐ ion the more 

salts are available. Na salts are  very  soluble, but the mixed salts  with Zn 

and Uranium can be used in quantitative analysis.

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Complexation of 

 Alakali

 Metals

The binding constants for  18‐crown‐6 : Li<Na,Cs<Rb<K

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Biological transporters

 for

 Na

 and

 K

 Valinomycin and Nonactin: small cyclic polypeptides are the carriers of  alkaline metals across membranes.

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Reaction summary

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Reaction summary

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Group 2A

 elements

 Group 2A elements are very reactive

 Valence electron configuration ns2

 Lose 2 valence electrons to form noble gas configuration

 Form ionic compounds containing M

2+

cations  Oxides are basic:

MO(s) + H2O(l)M2+(aq) + 2OH‐

(aq)

 Ca, Sr, and Ba react vigorously with water:

M(s) + 2H2O(l)M2+(aq) + 2OH‐

(aq) + H2(g)

 Be form covalent bond because of small size and high

electronegativity 

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Be structure

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2 e‐ 3

 center

 bond

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Mg Mg is intermediate in its behaviour between Be and 

the other elements in this group.

 Its chemistry  is entirely  ionic in nature.

 Mg: high

 polarization

 ability 

 The Hydroxides of  Be and Mg are only  slightly  soluble 

in  water.

 The other hydroxides of  this group are  water soluble 

and highly  basic.

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Ca, Sr,

 Ba,

 Ra

They  form a closely  related group  with the change in 

chemical and physical parameters follow a systematic 

change.

e.g. 

Electropositive nature increases from Ca‐>Ra.

Hydration energy  of  salts increase.

Insolubility  of  most salts, especially  sulfates increases in the same  way.

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Be 

and 

its 

compounds Be is obtained by  Ca or Mg reduction of  the BeCl2 or 

BeF2 salts.

 Be metal is relatively  unreactive. It does not react  with 

 water at red heat, and does not react  with air below 

600 deg C.

 Reaction  with air only  as fine powder  ‐> BeO, Be3N2.

 Be salts do not lose their  water molecules over strong 

desiccants 

(P2O5). Aqueous solutions of  Be salts are acidic 

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Mg production

 At 2000 degrees

Ca, Sr, Ba are made on a small scale from the Cl salts by  

reduction 

 with 

Na.

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Ion exchange

 Ca2+ and Mg2+ ions cause the hardness of water. These ions

of hard water interfere with the action of detergents andform precipitate with soap. Those ions are removed by ionexchange with ion exchange resins.

 Ca2+ and Mg2+ are often removed during ion exchange,releasing Na+ into solution.

 Ion exchange resin: large molecules that have many ionicsites.

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Group trends

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Group trends