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UNIT 2: Alkaline Earth Metals (Group IIA) ... 3
UNIT 6: Hydrogen - Oxygen - Sulfur (𝐻<small>2</small> – 𝑂<small>2</small> – 𝑆) ... 10
UNIT 8: Copper-Silver- Gold (𝐶𝑢 – – 𝐴𝑔 𝐴𝑢) (GROUP IB) ... 18
UNIT 10: Group VIB (CHROMIUN)... 28
UNIT 12: transition metal Iron-Cobalt-Nickel (𝐹𝑒 − 𝐶𝑜 − 𝑁𝑖) (GROUP VIIIB) ... 33
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<b>I. Experiment determinations: </b>
- The location of the alkalien-earth metals in the periodic table, their electron configuration, oxidation state and chemicals properties.
- Water hardness and method for softening water.
<b>II. Experimental Results: </b>
<b>1. Experiment 1: Observation of the color of alkaline earth metal flame </b>
<b>Produce: </b>
- Dip a clean filter paper into a saturated 𝐶𝑎𝐶𝑙<sub>2</sub> - Hold it over the flame
- Observe the color of the flame
- Repeat with saturated solutions of 𝑆𝑟𝐶𝑙<sub>2</sub>and 𝐵𝑎𝐶𝑙<sub>2</sub> Phenomenon of flame’s color:
o 𝐶𝑎𝐶𝑙<small>2</small>: orange-red o 𝑆𝑟𝐶𝑙<sub>2</sub>: red o 𝐵𝑎𝐶𝑙<sub>2</sub>: yellow-green
Explanation:
- When absorbing energy from the flame, electrons jump from lower energy level to higher one and then emitted energy in the form of photons to return to their initial states. Each
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different color's flame. Conclusion:
Burning alkaline-earth metal cation (in a compound with a suitable anion) will give specific flame color. In the group IIA, from top to bottom (Ca, Sr, Ba), the flame color will change from red to yellow, which can be understood by the increasing of energy due to the radius is increase, the electrons easily move to a higher energy level.
<b>2. Experiment 2: Reaction of an alkaline earth metal with H O <small>2</small></b>
Prepare 2 test tubes adding Observe the state of mixture and reaction at room temperature and the reaction occurs very slowly, the color of solution turns to light pink and s small
<b>amount of gas appears. </b>
- At high temperature, the reaction occurs quicker, the pink color becomes darker and spread throughout the solution, more gas
<b>appeared. </b>
- When 𝑁𝐻<small>4</small>𝐶𝑙 is added, the color of solution fades until it turns to colorless, at the same
- Creation of 𝐻<sub>2</sub> gas that escaped air bubbles and 𝑀𝑔(𝑂𝐻)<small>2</small> that covered the
<b>surface of Mg slows down the reaction. </b>
𝑀𝑔 + 2𝐻<small>2</small>𝑂 → 𝑀𝑔(𝑂𝐻)<sub>2</sub>+ 𝐻<sub>2</sub>
<small>- </small> Mg(OH)<small>2</small> dissolve partly in water, producing OH<small>-</small> that turning
phenolphthalein into pink at the interface between Mg and water.
𝑀𝑔( )𝑂𝐻<small>2</small>⇌𝑀𝑔<small>2+</small>+ 2𝑂𝐻<small>− </small> - At high temperature, 𝑀𝑔(𝑂𝐻)<sub>2</sub> is more
soluble in water, making the solution color darker. At the same time, the coverage of 𝑀𝑔( )𝑂𝐻<small>2</small> decreases making the first reaction occur stronger, creating more air bubbles.
- When 𝑁𝐻<small>4</small>𝐶𝑙 is added, it dissolves 𝑀𝑔(𝑂𝐻)<small>2</small>, which released the surface of Mg, making the reaction between Mg and
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time, more gas releases. After that, the solution turns to pink again.
𝐻<sub>2</sub>𝑂 occurred more stronger and increased the a mount of 𝐻<small>2</small> air bubbles. 𝑀𝑔(𝑂𝐻)<sub>2</sub>+ 𝑁𝐻<sub>4</sub>𝐶𝑙 ⇄ 𝑀𝑔𝐶𝑙<sub>2</sub>+ 𝑁𝐻<sub>3</sub>+ 𝐻<sub>2</sub>𝑂
- At the same time, 𝑀𝑔(𝑂𝐻)<small>2</small> is dissolved, the equilibrium of reaction is shifted to the backwards direction, which making 𝑂𝐻<small>−</small><sub> decrease therefore phenolphthalein </sub> turned back to being colorless. - Pink color reappears due to 𝑁𝐻<sub>3</sub> is
produced in the reaction and 𝑂𝐻<small>−</small> from the dissolution of 𝑀𝑔( )𝑂𝐻<small>2</small>.
<b>Conclusion: Alkaline-earth metals react weakly with water at room temperature, but react </b>
strongly when heated or in the presence of suitable catalyst.
<b>3. Experiment 3: Alkaline earth metal hydroxide synthesis 3.1) synthesis and properties of </b>𝑴𝒈(𝑶𝑯)<small>𝟐</small>
Synthesis 𝑀𝑔(𝑂𝐻)<sub>2</sub> from sodium hydroxide and magnesium salt, then centrifuge to get the solid. Decant the liquid and
- The precipitate absolute dissolved making the
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React with 𝑁𝑎𝑂𝐻 - Test tube 3:
React with 𝑁𝐻<sub>4</sub>𝐶𝑙
- The precipitate dissolved making the colorless solution, the pungent
- Prepare 4 separate test tubes containing 1 mL of 𝐵𝑎<small>2+</small>, 𝑆𝑟<small>2+</small>, 𝐶𝑎<small>2+</small>, 𝑀𝑔<small>2+</small> 0.5M solutions - Add 0.5 mL of 1M 𝑁𝑎𝑂𝐻 solution to each of test tubes
- Observe the formation of precipitate and compare the precipitate quantity Phenomenon:
- White precipitate created in all test tubes.
- The amount of precipitate increase in order of 𝐵𝑎<small>2+</small>, 𝑆𝑟<small>2+</small>, 𝐶𝑎<small>2+</small> and 𝑀𝑔<small>2+</small> Reactions and Explanation:
𝑀𝑔<small>2+</small>+ 2𝑂𝐻<small>−</small>⇄𝑀𝑔( )𝑂𝐻<small>2</small> 𝑆𝑟<small>2+</small>+ 2𝑂𝐻<small>−</small>⇄ ( )𝑆𝑟𝑂𝐻<sub>2</sub> 𝐶𝑎<small>2+</small>+ 2𝑂𝐻<small>−</small>⇄ ( )𝐶𝑎𝑂𝐻<sub>2</sub> 𝐵𝑎<small>2+</small>+ 2𝑂𝐻<small>−</small>⇄𝐵𝑎 𝑂𝐻( )<small>2</small>
From 𝑀𝑔 𝐵𝑎 to , the atomic radius increases leading to the decrease in the attractive force of nucleus on its valence electrons. Moreover, due to oxygen has a high electronegativity which pulls electrons to itself, making the hydroxyl group highly polar making it easy to be dissolved in water.
<b>Conclusion: Hydroxide of alkaline earth metals can be synthesized by the reaction between </b>
their soluble salt with strong basic hydroxide solution. From 𝑀𝑔 𝐵𝑎 to , the solubility of these hydroxide decreases.
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<b>salts </b>
1) Slowly add 0.5 mL of 2N sulfuric acid to 4 separate test tubes Then centrifuge . the solutions to observe the
- White precipitate but less than others
- The biggest amount of - From 𝑀𝑔 𝐵𝑎 to , the radius of ion
𝑋<small>2+</small><sub> increases, so the polarizability </sub> of it in water and hydrate energy decreases. Moreover, the activation of the cations is larger than lattice energy. From these reasons above, the solubility decreases from 𝑀𝑔 to 𝐵𝑎.
- When adding excess 𝐻<small>2</small>𝑆𝑂<small>4</small>, the concentration of 𝑆𝑂<sub>4</sub><small>2−</small><sub> increases, </sub> making the equilibrium shifts to the forward direction reaction, increasing the amount of precipitate.
<b>Conclusion: The solubility of alkaline earth metals decrease from </b>𝑀𝑔 𝐵𝑎 to .
<b>5. Experiment 5: Evaluation of water hardness </b>
Produce:
- Extract 10ml hard water by using pipet 10ml into 250ml erlenmeyer flask - Add distilled water in order to obtain around 100ml of volume in total. - Add 5ml buffer solution pH=10, add 4 to 7 drops of ERIO-T indicator color.
- Shake and titrate using 0.02N EDTA solution until the indicator color changes from purple-red to light blue
</div><span class="text_page_counter">Trang 8</span><div class="page_container" data-page="8"><b>Conclusion: The total remaining content of </b>𝑀𝑔<small>2+</small> and 𝐶𝑎<small>2+</small>is 14.6 (mN)
<b>6. Experiment 6: Water softening </b>
<b>Conclusion: </b>𝑋′ < 𝑋 meaning that the amount of 𝑀𝑔<small>2+</small> and 𝐶𝑎<small>2+</small> in sample decrease. Water is softened when 𝑁𝑎<sub>2</sub>𝐶𝑂<sub>2</sub> and 𝐶𝑎( )𝑂𝐻<sub>2</sub>is added.
𝑀𝑔<small>2+</small>+ 2𝑂𝐻<small>−</small>⇄𝑀𝑔( )𝑂𝐻<sub>2</sub> 𝐶𝑎<small>2+</small>+𝐶𝑂<sub>3</sub><small>2−</small>⇄ 𝐶𝑎𝐶𝑂<sub>3</sub>
<b>III. Questions </b>
<b>1. In reaction 2, explain the role of </b>𝑵𝑯<small>𝟒</small>𝑪𝒍<b>. Is it compulsory that </b>𝑵𝑯<small>𝟒</small>𝑪𝒍<b> be used or are other </b>𝑵𝑯<sub>𝟒</sub><b> salts also applicable? </b>
𝑁𝐻<sub>4</sub>𝐶𝑙 is added to react with 𝑀𝑔(𝑂𝐻)<sub>2</sub>, which covering the surface of 𝑀𝑔. Therefore, it makes the reaction between 𝑀𝑔 and 𝐻<sub>2</sub>𝑂 occurs more easily.
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𝑀𝑔(𝑂𝐻)<sub>2</sub>+ 𝑁𝐻<sub>4</sub>𝐶𝑙 ⇄ 𝑀𝑔𝐶𝑙<sub>2</sub>+ 𝑁𝐻<sub>3</sub>+ 𝐻<sub>2</sub>𝑂
Other 𝑁𝐻<small>4</small> salts also applicable because 𝐶𝑙<small>−</small> don’t have role in the reaction above. This reaction is basically between 𝑁𝐻<sub>4</sub><small>+</small> and 𝑂𝐻<small>−</small><sub>. </sub>
𝑁𝐻<sub>4</sub><small>+</small>+ 𝑂𝐻<small>−</small>⇄ 𝑁𝐻<small>3</small>+ 𝐻<small>2</small>𝑂
<b>2. Aside from using washing soda (</b>𝑵𝒂<sub>𝟐</sub>𝑪𝑶<sub>𝟑</sub><b>), are there any other methods for softening hard water? Write down the equation for each method. </b>
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- Preparation of hydrogen and oxygen gas: by water displacement method. - Chemical properties of hydrogen, oxygen, sulfur:
o Hydrogen: atomic hydrogen is a stronger reducing agent than molecular hydrogen. o Oxygen: oxygen is a strong oxidizing agent, easily oxidizing metals and non-metals
to form oxides. Oxygen also maintains combustion.
o Sulfur: at high temperature, sulfur has strong oxidizing properties.
<b>Experiment Description of interesting experiments and observations. </b>
<b>Explain the phenomenon, writing equation, analysis and conclusion </b>
<b>1. Synthesis of Hydrogen. </b>
- Install the air gathering system.
Introduce five pellets of zinc metal to the test tube prior to adding 5 𝑚𝐿 of concentrated 𝐻𝐶𝑙. Collect the gas produced with a small test tube filled with water upside down in a pot. Igniting the hydrogen gas released at the top of the pipe has
𝑍𝑛 + 2𝐻𝐶𝑙 → 𝐶𝑙𝑍𝑛 <small>2</small>+ 𝐻<small>2</small>↑
Because hydrogen reacts with oxygen mixed in the test tube and in the gas system, there is an explosion. Initially, the amount of oxygen was more, so there was a loud explosion.
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<b>Result: </b>
m<small>Morh’s salt weighed</small> = 12.83g m<small>Morh’s salt theory</small> = <small>5</small>
<b>2. Experiment 2: Properties of </b>𝑭𝒆<small>𝟐+</small><b> and </b>𝑭𝒆<small>𝟑+</small><b> compounds </b>
+ Tube 2: 𝐻<sub>2</sub>𝑂<sub>2</sub> solution which was previously acidized using
</div><span class="text_page_counter">Trang 36</span><div class="page_container" data-page="36">leftover, the melting cabinet creates a brown soil color that makes the starch turn blue.
2𝐹𝑒<small>3+</small> + 𝐼 →<small>−</small> 𝐹𝑒<small>2+</small> + 𝐼<small>2</small> (charcoal purple) - When KI is excess:
𝐼<sub>2</sub> + → 𝐾𝐼𝐾𝐼 <sub>3</sub> (brown soil)
</div><span class="text_page_counter">Trang 37</span><div class="page_container" data-page="37">- 𝐹𝑒<small>3+</small><b><sub> salt is stable in the air and has oxidation property in acids. </sub></b>
<b>3. Experiment 3: Properties of </b>𝑪𝒐<small>𝟐+</small><b>and </b>𝑵𝒊<small>𝟐+</small><b> compounds </b>
- Add 5 drops 𝐶𝑜𝐶𝑙<sub>2</sub> and add few drops 2N 𝑁𝑎𝑂𝐻 to 2 test tubes
- The solution’s color is pink. - Blue precipitate appears and changes to the red color
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- Put in 2 test tubes each 5
The color stays unchanged
Air bubbles appear
Precipitate turns gray
Precipitation turns gray and air
</div><span class="text_page_counter">Trang 39</span><div class="page_container" data-page="39">+ Part 1: The precipitate dissolves and creates a yellow
+ Part 1: The precipitate dissolved slightly to create a light pink solution
</div><span class="text_page_counter">Trang 40</span><div class="page_container" data-page="40">- Green precipitate appears.
+ Part 1: The precipitate dissolved to create a pale pink solution
+ Part 2: No phenomenon
𝑁𝑖<small>2+</small> + 2𝑂𝐻<small>−</small> → 𝑁𝑖(𝑂𝐻)<small>2</small> ( green)
𝑁𝑖(𝑂𝐻)<small>2</small>+ 𝐻 → <small>+</small> 𝑁𝑖<small>2+</small> + 2𝐻<small>2</small>𝑂
Before adding HCl and NaOH:
After adding HCl and NaOH:
</div><span class="text_page_counter">Trang 41</span><div class="page_container" data-page="41">- In alkali, hydroxides are more stable and insoluble.
<b>4. Experiment 4: Properties of </b>𝑪𝒐<small>𝟐+</small><b>and </b>𝑵𝒊<small>𝟐+</small><b>compounds </b>
<b>The color change of </b>𝑪𝒐<small>𝟐+</small>
- Write letters on filter paper and view the letter color. Dry filter paper by flame.
<b>The Tsugaep reaction of Nickel:</b>
- The letters’s color is pink. Drying by the flames of alcohol lamps. The pink color disappears and the blue purple – color appears instead.
- In the heating process, complex 𝐶𝑜(𝐻<small>2</small>𝑂)<small>6</small><sup>2+</sup> loses water to form a smaller complex 𝐶𝑜(𝐻<sub>2</sub>𝑂)<sub>4</sub><small>2+</small><sub> having a blue </sub>– purple color.
𝑁𝑖<small>2+</small> + 2𝑂𝐻<small>−</small> → 𝑁𝑖(𝑂𝐻)<small>2</small>(green)
</div><span class="text_page_counter">Trang 42</span><div class="page_container" data-page="42">- Green precipitate appears then dissolves to creates a dark blue
- The 𝑁𝑖(𝐶<sub>4</sub>𝐻<sub>7</sub>𝑁<sub>2</sub>𝑂<sub>2</sub>)<sub>2</sub> complex has a square shape with weak acidity and basicity in the water or in the diluted NH<small>4</small>OH solution, but it dissolves well in strong acid and base.
<b>Conclusion: </b>
- The complex has a square shape with weak acidity and basicity in the water or in the diluted 𝑁𝐻<sub>4</sub>𝑂𝐻 solution, but it dissolves well in strong acid and base. Therefore, when replacing 𝑁𝐻<small>4</small>𝑂𝐻 with 𝑁𝑎𝑂𝐻, the enough amount will lead to an appearane of the light red precipitate. On the contrary, adding excess 𝑁𝑎𝑂𝐻 could make the precipitate dissolve immediately. - The Tsugaep reaction is used to calculate and quantify 𝑁𝑖<small>2+</small> in the solution.
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<b>5. Experiment 5: Properties of </b>𝑪𝒐<small>𝟐+</small><b> and </b>𝑵𝒊<small>𝟐+</small><b> compou<sub>nds</sub></b>
Pink precipitate appears then dissolves shortly afterwards, create a brown solution above, pink below and blue in the middle. When vigorously shaken, the entire solution turns brown.
The solution turns blue
Blue precipitate appears and create a dark blue solution
𝐶𝑜<small>2+</small>+ 2𝑂𝐻<small>−</small>→ (𝑂𝐻)𝐶𝑜 <small>2</small> (pink) 𝐶𝑜(𝑂𝐻)<small>2</small>+ 6 𝑁𝐻<small>3</small> →
[𝐶𝑜(𝑁𝐻<sub>3</sub>)<sub>6</sub>](𝑂𝐻) (brown) <sub>2</sub> The blue color appears because the concentrated 𝑁𝐻<sub>4</sub>𝑂𝐻 absorbs water from on
</div><span class="text_page_counter">Trang 44</span><div class="page_container" data-page="44">- 𝑁𝑖(𝑂𝐻)<small>2</small> and 𝐶𝑜(𝑂𝐻)<small>2</small> are soluble in 𝑁𝐻<small>3</small><b> due to their ablility to form stable complexes. </b>
- Both 𝐶𝑜<small>2+</small><sub> and </sub>𝑁𝑖<small>2+</small><sub> are able to form complexes with </sub>𝐶𝑙<small>−</small><sub> and those complexes may change </sub>
<b>the color of solution. </b>
<b>III. Questions: </b>
<b>1. How are two-valent and three-valent salts synthesized from Fe metal? Write down the reaction equations. </b>
<b>2. How is double salt different from complex salt? </b>
A mixture of many salts that crystallize at the same time.
A compound.
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force between salt molecules. between the central ions and the ligands. Exist in solid form and dissolve
into constituent species in solution.
Exist In both solid and liquid states and still maintain their identity.
Completely dissociate into its ions in
<b>3. What ions are present in the Morh’s salt solution? </b>
The Morh’s salt solution is 𝐹𝑒𝑆𝑂<small>4</small>(𝑁𝐻<small>4</small>)<small>2</small>𝑆𝑂<small>4</small>. 6𝐻<small>2</small>𝑂.
- After dissolving the Morh’s salt in water, two 𝑁𝐻<sub>4</sub><small>+</small>, two 𝑆𝑂<sub>4</sub><small>2−</small><sub>and one </sub>𝐹𝑒<small>2+</small><sub> will be </sub> produced. To prove that:
- Add concentrated 𝑁𝑎𝑂𝐻 solution and heat gently 𝐹𝑒<small>2+</small> + 2𝑂𝐻<small>−</small> → 𝐹𝑒(𝑂𝐻)<small>2</small>
4𝐹𝑒(𝑂𝐻)<small>2</small>+ 𝑂 + 2𝐻<sub>2</sub> <sub>2</sub>𝑂 → 4𝐹𝑒(𝑂𝐻)<sub>3</sub>
- There is a mossy green precipitate that rapidly turns brown in the air The presence of 𝐹𝑒<small>2+</small><sub>. </sub> - There is a presence of urine gas The presence of 𝑁𝐻<sub>4</sub><small>+</small>
𝑁𝐻<sub>4</sub><small>+</small> +𝑂𝐻<small>−</small> →𝑁𝐻<sub>3</sub>+ 𝐻<sub>2</sub>𝑂 - Add 𝐵𝑎𝐶𝑙<sub>2</sub> salt solution
𝐵𝑎<small>2+</small> + 𝑆𝑂<sub>4</sub><small>2−</small>→ 𝐵𝑎𝑆𝑂<sub>4</sub>
- A white precipitate is formed that is insoluble in strong acids The presence of 𝑆𝑂<sub>4</sub><small>2−</small>
<b>4. Explain the procedure for the synthesis of Morh’s salt solution. </b>
Dissolve Fe in dilute 𝐻<sub>2</sub>𝑆𝑂<sub>4</sub> to form 𝐹𝑒<small>2+</small>. The heating speeds up the dissolution reaction and it also makes 𝐻<small>2</small>𝑆𝑂<small>4</small> become denser, which will oxidize 𝐹𝑒<small>2+</small> to 𝐹𝑒<small>3+</small>.
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Therefore, it is necessary to regularly add water to dilute H<small>2</small>SO<small>4</small> to limit 𝐹𝑒<small>3+</small> formation and keep excess 𝐹𝑒 to convert 𝐹𝑒<small>3+</small> to 𝐹𝑒<small>2+</small><sub>. </sub>
When excess Fe is almost gone, filter to remove impurities. Immediately add solid (𝑁𝐻<sub>4 2</sub>) 𝑆𝑂<sub>4</sub>to the becher to collect filtered water and stir well to create two saturated copper salt solutions so that the two salt solutions can crystallize at the same time. (𝑁𝐻<small>4</small>)<small>2</small>𝑆𝑂<small>4</small> act as a reducing agent that will keep 𝐹𝑒<small>2+</small><sub>: </sub> from being oxidized to 𝐹𝑒<small>3+</small> in the double salt. Soak the becher in cold water for a more favorable crystallization process.
<b>5. What reactions are used to detect the presence of </b>𝑭𝒆<small>𝟐+</small><b> and </b>𝑭𝒆<small>𝟑+</small><b><sub>? </sub></b>
For the detection of 𝐹𝑒<small>2+</small>: 𝐹𝑒<small>2+</small> reacts with potassium ferricyanide will form the turnbull blue precipitate of ferrous ferricyanide.
3𝐹𝑒<small>2+</small> + 2[𝐹𝑒(𝐶𝑁)<sub>6</sub>]<small>3−</small> → 𝐹𝑒 𝐹𝑒<sub>3</sub>[ ( )𝐶𝑁<sub>6</sub>]<sub>2</sub>
For detection of Fe : Fe reacts with potassium ferrocyanide to form potassium berlin blue <small>3+3+</small> precipitate of ferric ferrocyanide.
4𝐹𝑒<small>3+</small>+ 3[𝐹𝑒(𝐶𝑁)<small>6</small>]<small>4−</small>→ 𝐹𝑒<small>4</small>[𝐹𝑒( )𝐶𝑁 ]<small>63</small>
<b>6. What kind of reaction as conducted in the experiment 4b? What is it used for? </b>
The Tsugaep reaction is a complexation reaction of 𝑁𝑖( )𝐼𝐼: nickel dimethylglyoximatein dilute 𝑁𝐻<sub>3</sub> solution, used for qualitative and quantitative determination of Ni in solution. <small>2+</small>
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