a) `AlCl_3` fumes in moist air due to its hydrolysis
b) Al metal is stable in dry air because of protective oxide layer.
c) `p pi -p pi` back bonding does not occur in halides of aluminium because of larger size.
d) Anhydrous `AlCl_3` cannot be prepared by heating `AlCl_3 . 6H_2 O`.
Correct statements are
a) `AlCl_3` fumes in moist air due to its hydrolysis
b) Al metal is stable in dry air because of protective oxide layer.
c) `p pi -p pi` back bonding does not occur in halides of aluminium because of larger size.
d) Anhydrous `AlCl_3` cannot be prepared by heating `AlCl_3 . 6H_2 O`.
Correct statements are
b) Al metal is stable in dry air because of protective oxide layer.
c) `p pi -p pi` back bonding does not occur in halides of aluminium because of larger size.
d) Anhydrous `AlCl_3` cannot be prepared by heating `AlCl_3 . 6H_2 O`.
Correct statements are
A
a , b only
B
b,c only
C
a,c,d only
D
All of these
Text Solution
AI Generated Solution
The correct Answer is:
To determine which statements about aluminum chloride and aluminum are correct, let's analyze each statement step by step.
### Step 1: Analyze Statement A
**Statement A:** `AlCl_3` fumes in moist air due to its hydrolysis.
- **Explanation:** Aluminum chloride (AlCl₃) reacts with water in moist air to form aluminum hydroxide and hydrochloric acid. The reaction can be represented as:
\[
\text{AlCl}_3 + 3 \text{H}_2\text{O} \rightarrow \text{Al(OH)}_3 + 3 \text{HCl}
\]
- The hydrochloric acid produced is responsible for the white fumes observed. Therefore, this statement is **correct**.
### Step 2: Analyze Statement B
**Statement B:** Al metal is stable in dry air because of the protective oxide layer.
- **Explanation:** Aluminum metal reacts with oxygen in the air to form a thin layer of aluminum oxide (Al₂O₃) on its surface. This oxide layer protects the underlying aluminum from further oxidation, making it stable in dry air. Thus, this statement is also **correct**.
### Step 3: Analyze Statement C
**Statement C:** `p pi - p pi` back bonding does not occur in halides of aluminum because of larger size.
- **Explanation:** In compounds like BF₃, back bonding occurs due to the small size of boron, allowing effective overlap of p orbitals. However, aluminum is larger, and thus, it does not exhibit significant p pi - p pi back bonding in its halides. Therefore, this statement is **correct**.
### Step 4: Analyze Statement D
**Statement D:** Anhydrous `AlCl_3` cannot be prepared by heating `AlCl_3 . 6H_2 O`.
- **Explanation:** When heating AlCl₃·6H₂O, the reaction produces aluminum hydroxide and hydrochloric acid rather than anhydrous aluminum chloride. The balanced equation is:
\[
2 \text{AlCl}_3 \cdot 6 \text{H}_2\text{O} \rightarrow 2 \text{Al(OH)}_3 + 6 \text{HCl}
\]
- Since anhydrous AlCl₃ is not produced, this statement is also **correct**.
### Conclusion
All four statements (A, B, C, and D) are correct.
### Final Answer
The correct statements are: **All of the above (A, B, C, D)**.
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Similar Questions
Explore conceptually related problems
Give reasons for the following (a) No visible reaction occurs when aluminium is left in contact with conc HNO_(3) . (b) The hydroxides of Al and Fe are insoluble in water. However, NaOH is used to distinguish one from another. ( c) Anhydrous AlCl_(3) cannot prepared by heating hydrated aluminium chloride. (d) Aluminium vessels should not be cleaned with cleansing agent containing washing soda. ( e) Duralumin is used in aircraft industry.
The small size and high charge of Al^(3+) ion gives it a high charge density which is responsible for its tendency to show (a) covalency in its compounds in the gaseous state (b) high hydration energy which stabilizes its compounds in solution, and (c) high lattice energy of its compounds in the solid state. Thus aluminium can forms both covalent and ionic bond. Like halides of boron, halides of aluminium do not show back bonding because of increase in size of aluminium. Actually aluminium atoms complete their octets by forming dimers. Thus chloride and bromide of aluminium exist as dimers, both in the vapour state and in polar-solvents like benzene while the corresponding boron halides exists as monomer. In boron trihalides the extent of back bonding decreases with increases with increase in size of halogens and thus lewis acid character increases. All BX_(3) are hydrolysed by water but BF_(3) shows a different behaviour. Which of the following statements about anhydrous aluminium chloride is correct ?
The small size and high charge of Al^(3+) ion gives it a high charge density which is responsible for its tendency to show (a) covalency in its compounds in the gaseous state (b) high hydration energy which stabilizes its compounds in solution, and (c) high lattice energy of its compounds in the solid state. Thus aluminium can forms both covalent and ionic bond. Like halides of boron, halides of aluminium do not show back bonding because of increase in size of aluminium. Actually aluminium atoms complete their octets by forming dimers. Thus chloride and bromide of aluminium exist as dimers, both in the vapour state and in polar-solvents like benzene while the corresponding boron halides exists as monomer. In boron trihalides the extent of back bonding decreases with increases with increase in size of halogens and thus lewis acid character increases. All BX_(3) are hydrolysed by water but BF_(3) shows a different behaviour. Which of the following reaction is incorrect ?
Despite the fact that aluminium is a reactive metal, it is a stable in air as well as in water. This is due to the formation of thin layer of oxide on the surface of aluminium metal which makes it passive for further attack. The layer is so useful, that in industry, it is purposely deposited by an electrolytic process called anodising. Reaction of aluminium with oxygen is highly exothermic and is called thermite reaction. 2Al_((s)) +(3)/(2) O_(2(g)) rarr Al_(2)O_(3(s)) Delta_(f) H^(Ө) = -1670 kJmol^-1 This reaction finds application for welding of metal and in the metallurgical extraction of many metals from their oxides. The limitation is that to start the reaction, high temperature is required for which an ignition mixture is required. Which of the following metals cannot be extracted by using Al as a reducing agent ?
Despite the fact that aluminium is a reactive metal, it is a stable in air as well as in water. This is due to the formation of thin layer of oxide on the surface of aluminium metal which makes it passive for further attack. The layer is so useful, that in industry, it is purposely deposited by an electrolytic process called anodising. Reaction of aluminium with oxygen is highly exothermic and is called thermite reaction. 2Al_((s)) +(3)/(2) O_(2(g)) rarr Al_(2)O_(3(s)) Delta_(f) H^(Ө) = -1670 kJmol^-1 This reaction finds application for welding of metal and in the metallurgical extraction of many metals from their oxides. The limitation is that to start the reaction, high temperature is required for which an ignition mixture is required. Anodising can be done by elecrolysing dil H_(2)SO_(4) with Al as anode. This results in :
Despite the fact that aluminium is a reactive metal, it is a stable in air as well as in water. This is due to the formation of thin layer of oxide on the surface of aluminium metal which makes it passive for further attack. The layer is so useful, that in industry, it is purposely deposited by an electrolytic process called anodising. Reaction of aluminium with oxygen is highly exothermic and is called thermite reaction. 2Al_((s)) +(3)/(2) O_(2(g)) rarr Al_(2)O_(3(s)) Delta_(f) H^(Ө) = -1670 kJmol^-1 This reaction finds application for welding of metal and in the metallurgical extraction of many metals from their oxides. The limitation is that to start the reaction, high temperature is required for which an ignition mixture is required. Aluminium becomes passive in :
Despite the fact that aluminium is a reactive metal, it is a stable in air as well as in water. This is due to the formation of thin layer of oxide on the surface of aluminium metal which makes it passive for further attack. The layer is so useful, that in industry, it is purposely deposited by an electrolytic process called anodising. Reaction of aluminium with oxygen is highly exothermic and is called thermite reaction. 2Al_((s)) +(3)/(2) O_(2(g)) rarr Al_(2)O_(3(s)) Delta_(f) H^(Ө) = -1670 kJmol^-1 This reaction finds application for welding of metal and in the metallurgical extraction of many metals from their oxides. The limitation is that to start the reaction, high temperature is required for which an ignition mixture is required. Anodised aluminium is.
Despite the fact that aluminium is a reactive metal, it is a stable in air as well as in water. This is due to the formation of thin layer of oxide on the surface of aluminium metal which makes it passive for further attack. The layer is so useful, that in industry, it is purposely deposited by an electrolytic process called anodising. Reaction of aluminium with oxygen is highly exothermic and is called thermite reaction. 2Al_((s)) +(3)/(2) O_(2(g)) rarr Al_(2)O_(3(s)) Delta_(f) H^(Ө) = -1670 kJmol^-1 This reaction finds application for welding of metal and in the metallurgical extraction of many metals from their oxides. The limitation is that to start the reaction, high temperature is required for which an ignition mixture is required. The reaction which is not involved in thermite process is
Despite the fact that aluminium is a reactive metal, it is a stable in air as well as in water. This is due to the formation of thin layer of oxide on the surface of aluminium metal which makes it passive for further attack. The layer is so useful, that in industry, it is purposely deposited by an electrolytic process called anodising. Reaction of aluminium with oxygen is highly exothermic and is called thermite reaction. 2Al_((s)) +(3)/(2) O_(2(g)) rarr Al_(2)O_(3(s)) Delta_(f) H^(Ө) = -1670 kJmol^-1 This reaction finds application for welding of metal and in the metallurgical extraction of many metals from their oxides. The limitation is that to start the reaction, high temperature is required for which an ignition mixture is required. Thermite mixture used for welding is
When an atom or an ion is missing from its nomal lattice site a lattice vacanecy (Schottky defect) is created. In stoichmeteric ionic crystals, a vacancy of one ion has to be accompanied by the vacancy of the oppositely charge ion in order to maintain electrical neutrality. In a Frenkel defect an ion leaves its position in the lattice and occupies an interstitial void. This id the Frenkel defect commonly found along with the Schottky defects and interstitial. In pure alkali halides. Frenked defects are not found since the ions cannot get into the interstitial sites. Frenkel defects are found in silver halides because of the small size of the Ag^(+) ion. Unike Schottky defects, Frenkel defect do not change the density of the solids. in certain ionic solids (e.g., AgBr) both schottky and Frenkel defect occur. The Defects idiscussed above do not disturb the stoichiometery of the crystalline material. there is large variety of non-stoichiometric inorganic solids which contains an excess or deficienty of one of the elements. Such solids showing deviations from the ideal stoichiometric composition from an important group of solids. For example in the vanadium oxide, VO_(x),x can be anywehere between 0.6 and 1.3 there are solids such as difficult to prepare in the soichiometric omposition thus, the ideal composition in compounds such as FeO is difficult to obtain (normally we get a compositiion of Fe(0.95) O but it may range from Fe_(0.93) O to Fe_(0.96)O ). Non-stoichiometric behavious is most commonly found for transition metal compounds through is also known for some lathanoids and actinoids. Zinc oxide loses oxygen reversible at high temperature and turns yellow in colour. the excess metal is accomodated interstitial, giving rise to electrons trapped in the neighbourhood, the enchanced electrical conductivity of the non-stoichiometric ZnO arises from these electrons. Anion vacancies in alkali halides are produced by heating the alkali halid crystals in an atmosphere of the alkali metal vapour. when the metal atoms deposit on the surface they diffuse into the cystal and after ionisation the alkali metal ion occupies cationic vacancy whereas electron occupies anionic vacancy. Electrons trapped i anion vacancies are referred to as F-centers (From Farbe the German word for colouf) that gives rise to interesting colour in alkali halides. Thus, the excess of potassium i KCl makes the crystal appear violet and the excess of lithium in LiCl makes it pink. Which of the following is most appropritate crystal to show Fremkel defect ?
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