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Potassium Reactivity in Water Reactions

The document discusses reactivity series and reactions of metals. It explains that the reactivity series lists elements in order of their reactivity, with more reactive elements at the top. Metals at the top of the series, like potassium, react vigorously with water and acids. Less reactive metals form protective oxide coatings that slow their reactions. The document also covers displacement reactions, oxidation/reduction, and factors that influence the rusting of iron.

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0% found this document useful (0 votes)
11 views5 pages

Potassium Reactivity in Water Reactions

The document discusses reactivity series and reactions of metals. It explains that the reactivity series lists elements in order of their reactivity, with more reactive elements at the top. Metals at the top of the series, like potassium, react vigorously with water and acids. Less reactive metals form protective oxide coatings that slow their reactions. The document also covers displacement reactions, oxidation/reduction, and factors that influence the rusting of iron.

Uploaded by

Mia Poon
Copyright
© All Rights Reserved
We take content rights seriously. If you suspect this is your content, claim it here.
Available Formats
Download as DOCX, PDF, TXT or read online on Scribd

Chapter 14: Reactivity Series

14.1 The Reactivity Series


 Elements- decreasing reactivity
 Higher position- more reactive it’s

14.2 Reactions of metals with water & steam


 Metal+ water -> metal hydroxide + hydrogen
 Metal+ water -> metal oxide + hydrogen

Reactions with water, H2O(l)

Potassium (K)
 A lilac flame is seen, melts into a slivery white ball, with a hissing sound, white trails
KOH is seen
2 K(s) + 2 H2O(l) -> 2 KOH(aq) + H2(g)

Sodium (Na)
 Similar but slower reaction. No flame
2 Na(s)+ 2 H2O(l) -> 2 NaOH(aq) + H2(g)

Lithium (Li)
 Similar but even slower reaction. Li doesn’t melt
2 Li(s) + 2 H2O(l) -> 2 LiOH(aq) + H2(g)

Calcium (Ca)
 Ca(OH)2 is slightly soluble in water. A white suspension & colorless gas bubbles are
formed
 Becomes warm as the reaction is exothermic
Ca(s) + 2 H2O(l) -> Ca(OH)2(s) + H2(g)

Magnesium (Mg)
 Coated with insoluble Mg(OH)2, prevents more water coming into contact with Mg
Mg(s) + 2 H2O(g) -> Mg(OH)2(s) + H2(g)

Reactions with steam, H2O(g)

Magnesium (Mg)
 Burns with a bright white flame, a white powder is formed
Mg(s) + H2O(l) -> MgO(s) + H2(g)

Aluminium (Al)
 Slow reaction, covered in a very thin but tough layer of Al2O3
2 Al(s) + 3 H2O(g) -> Al2O3(s) + 3H2(g)

Zinc (Zn)
 A yellow solid when hot but white on cooling
Zn(s) + H2O(g) -> ZnO(s) + H2(g)

Iron (Fe)
 Fe3O4, dark grey solid
3 Fe(s) + 4 H2O(g) -> Fe3O4(s) + 4 H2(g)

14.3 Reactions of metals with dilute acids


 Metal + dilute sulphuric acid -> metal sulphate + hydrogen
 Metal + dilute hydrochloric acid -> metal chloride + hydrogen

Reactions with dilute hydrochloric acid, HCl(aq)

Calcium (Ca)
 Colorless gas bubbles are formed
Ca(s) + 2 HCl(aq) -> CaCl2(aq) + H2(g)

Magnesium (Mg)
Mg(s) + 2 HCl(aq) -> MgCl2(aq) + H2(g)

Aluminium (Al)
2 Al(s) + 6 HCl(aq) -> 2 AlCl3(aq) + 3 H2(g)

Zinc (Zn)
Zn(s) + 2 HCl(aq) -> ZnCl2(aq) + H2(g)

Iron (Fe)
 Pale green solution
Fe(s) + 2 HCl(aq) -> FeCl2(aq) + H2(g)

Lead (Pb)
 Colorless gas bubbles can be seen before the reaction stops
 Pb is coated with insoluble PbCl2, prevent more acid coming into contact with Pb
Pb(s) + 2 HCl(aq) -> PbCl2(s) + H2(g)

Reactions with dilute sulphuric acid, H2SO4(aq)

Calcium (Ca)
Ca(s) + H2SO4(aq) -> CaSO4(s) + H2(g)

Magnesium (Mg)
Mg(s) + H2SO4(aq) -> MgSO4(aq) + H2(g)

Aluminium (Al)
2 Al(s) + 3 H2SO4(aq) -> Al2(SO4)3(aq) + 3 H2(g)

Zinc (Zn)
Zn(s) + H2SO4(aq) -> ZnSO4(aq) + H2(g)
Iron (Fe)
Fe(s) + H2SO4(aq) -> FeSO4(aq) + H2(g)

Lead (Pb)
Pb(s) + H2SO4(aq) -> PbSO4(s) + H2(g)

14.4 Oxidation and reduction


 A redox reaction is one which both reduction & oxidation are occurring

Oxidation
 Gain of oxygen, loss of electrons

Reduction
 Loss of oxygen, gain of electrons

Reducing agent
 By transfer electron or by accepting oxygen

Oxidizing agent
 By accepting electron or by transferring oxygen

Example: 2 Fe + 3 Cl2 -> 2 FeCl3


 When iron reacts with chlorine to form FeCl3, It undergoes oxidation as it loses
electrons to form Fe3+ ions

14.5 Displacement reactions involving metal oxide


A more reactive metal can displace a less reactive one from its oxide

More reactive metal + oxide of less reactive metal -> oxide of more reactive metal + less
reactive metal

Example: Mg(s) + CuO(s) -> MgO(s) + Cu(s)

Types of reaction: displacement


 Mg displaces Cu from CuO because Mg is more reactive than Cu

Observable change:
 A mixture of white solid & brown solid is resulted

State with explanation, which substance is oxidized and which one is reduced
 Mg is oxidized as it gains O
 CuO is reduced as it loses O

State with explanation, which substance acts as the oxidizing aganet and which one acts as
the reducing agent
 CuO acts as the oxidizing agent as it oxidizes Mg by transferring O to it
 Mg acts as the reducing agent as it reduces CuO by accepting O from it
14.7 Ionic equations and ionic half equations (self-study from notes)

14.8 Colors of common solids and common ions in aqueous solutions

Solid Color
most metals Slivery grey
Cu brown
K, Na, Li, Ca, Mg & Al white
ZnO Yellow when hot, white when cold
Oxides of Fe Dark grey/ black
C/ CuO black
Ag2O Dark brown

Blue: Cu2+
Green: Fe2+, Ni2+, Cr3+
Orange: Cr2O72-
Yellow: Fe3+, CrO42-
Pink: Mn2+
Purple: MnO4-

14.9 Rusting of iron


 a metal corrodes when it reacts with air, water or other substances in the
surrounding and gradually become deteriorated
 slow chemical process

What is rust?
 A reddish brown solid
 Hydrated iron (III)oxide
 Fe2O3 x xH2O
Necessary conditions for rusting: oxygen & water

Factors that speed up rusting


 Presence of electrolytes
 High temperature-> increase the rate of chemical reactions
 In contact with a less reactive metal

14.10 Rust prevention methods


 Preventing iron from losing electrons

Barrier methods

Painting, coating with plastic, oiling


 Serves as a barrier to prevent the iron object from contract with water& oxygen
 Economical, lasts long
Tin-plating
 Disadvantage: Fe is connected to a less reactive metal, it loses electrons & rusts
quickly

Zinc-plating
 Zinc is more reactive, loses electrons to any Fe2+ formed, prevented from losing
electrons
 Has a beautiful shiny appearance
 But zinc ions are poisonous, expensive

Preventing iron from losing electrons

Electrical protection (connect the iron project to the negative terminal)


 As the negative terminal supplies electrons to the iron object. Fe is prevented from
losing electrons

Rusting can be observed using rust


indicator (yellow)

Common questions

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Understanding the reactivity series allows for selecting metals with appropriate tendencies to donate electrons to act as reducing agents. More reactive metals, higher on the reactivity series, are better reducing agents because they are more inclined to lose electrons and reduce other substances. For example, magnesium can act as an effective reducing agent in displacing less reactive metals like copper from their compounds due to its high reactivity .

Tin plating prevents rust through a barrier method, covering iron from direct exposure to oxygen and water. However, a significant disadvantage is that if the tin layer is damaged, the underlying iron will corrode rapidly, as tin is less reactive, making iron the anodic site, which speeds up corrosion. In contrast, zinc plating not only acts as a physical barrier but also provides sacrificial protection. Zinc is more reactive than iron and, even when scratched, it will preferentially oxidize, protecting the iron beneath. The drawbacks include higher cost and potential toxicity of zinc ions .

Magnesium reacts differently with water compared to more reactive metals like potassium and sodium due to its lower reactivity. With water, magnesium forms an insoluble layer of Mg(OH)2 on its surface, which prevents further reaction as water cannot reach the metal core. In contrast, with steam, magnesium reacts more readily because the higher energy of steam facilitates the reaction, producing a bright white flame and forming MgO as a powder .

Iron oxidation during rusting represents a chemical problem due to the slow but inevitable degradation of iron objects, resulting in a loss of material integrity and functionality. Environmentally, rusting contributes to the deterioration of infrastructure, potentially leading to safety hazards and increased economic costs for repair and replacement. Additionally, rust formation on iron-rich industrial sites can complicate recycling and disposal processes, posing further environmental challenges .

In the reaction between magnesium and copper(II) oxide, oxidation and reduction occur simultaneously, illustrating a redox reaction. Magnesium is oxidized as it gains oxygen to form MgO, and copper(II) oxide is reduced as it loses oxygen to form copper metal. Thus, Mg acts as the reducing agent by donating oxygen to CuO, which serves as the oxidizing agent .

Displacement reactions are fundamental in extracting metals from their oxides by utilizing a more reactive metal to reduce the oxide of a less reactive one. The more reactive metal acts as a reducing agent, giving up its electrons to the oxide ions, reducing them to the elemental state. For example, magnesium can displace copper from copper(II) oxide, demonstrating this principle. This kind of displacement is energetically favorable for industry as it allows for selective extraction of desired metals using readily available and cost-effective reducing agents .

Electrolytes accelerate the rusting process of iron because they enhance the conductivity of the aqueous medium surrounding the metal. This increased conductivity facilitates the flow of electrons between anodic and cathodic sites on the iron surface, thereby accelerating the electrochemical reactions involved in rusting. For instance, in an electrolyte-rich environment, ions that partake in the corrosion process can move more freely, increasing the rate at which oxidation and reduction reactions occur, leading to quicker rust formation .

Electrical protection, or cathodic protection, is effective in preventing rusting by making the iron the cathode of an electrochemical cell, thereby preventing it from losing electrons. This method can dramatically slow down the rusting process and is particularly useful for protecting large structures like pipelines and ship hulls. However, this technique can have environmental impacts, such as the use and disposal of anodes and the potential for disturbing natural ion balances in aquatic environments where they are deployed. Despite these concerns, electrical protection remains a viable method due to its effectiveness .

Calcium hydroxide forms as a suspension because it is only slightly soluble in water. When calcium reacts with water, some calcium hydroxide precipitates out of the aqueous solution because its solubility is exceeded, forming visible solid particles suspended in the remaining liquid. This results in a white suspension while hydrogen gas is also evolved due to the exothermic nature of the reaction .

Aluminum's natural oxide layer, Al2O3, significantly reduces its reactivity with both acids and water by acting as a barrier that protects the underlying metal. This layer is very thin but tough, making aluminum appear unreactive in many conditions where bare metal would react. For instance, with water or dilute acids, aluminum reacts slowly because the oxide layer needs to be breached or dissolved first .

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