- A. Powdered salt in cold water
- B. Powdered salt in hot water
- C. Salt crystals in cold water
- D. Salt crystals in hot water
The dissolution of ammonium chloride is an endothermic process (indicated by the solution feeling cool). According to Le Chatelier's principle, increasing the temperature favours the endothermic direction, thus increasing solubility. Furthermore, powdered salt increases the surface area compared to crystals, leading to a faster rate of dissolution. Therefore, powdered salt in hot water is the ideal condition.
- A. atomic number
- B. shielding by 4f electrons
- C. effective nuclear charge
- D. atomic radius
Lanthanoid contraction refers to the steady decrease in atomic and ionic radii of lanthanoids as the atomic number increases. This is primarily due to the poor shielding effect of 4f electrons, which allows the effective nuclear charge to exert a greater pull on the outer shell electrons, drawing them closer to the nucleus.
- A. CH3COONa
- B. CH3NH2
- C. CH3CH2Br
- D. CH3CH2NH2
The reaction of an amide (CH3CONH2) with NaOH and Br2 is the Hofmann bromamide degradation reaction. This reaction converts a primary amide into a primary amine with one carbon atom less than the original amide. Thus, CH3CONH2 (acetamide) yields CH3NH2 (methanamine).
- A. 1 < 2 < 3
- B. 1 > 3 > 2
- C. 1 > 2 > 3
- D. 3 > 1 > 2
The reaction of alcohol with HCl in the presence of ZnCl2 is known as the Lucas test. This reaction proceeds via the formation of a carbocation intermediate. Tertiary (3°) alcohols form stable carbocations easily, followed by secondary (2°), and then primary (1°) alcohols. Thus, the order of reactivity is 3° > 2° > 1°, or 1 < 2 < 3.
- A. optical isomerism
- B. linkage isomerism
- C. ionisation isomerism
- D. coordination isomerism
Ionisation isomerism occurs when the counter ion in a coordination compound is a potential ligand and can displace a ligand which can then become the counter ion. Here, the sulphate ion (SO4^2-) and the bromide ion (Br-) exchange positions between the coordination sphere and the counter ion position.
- A. (CH3)2NH
- B. NH3
- C. NH2
- D. (CH3)3N
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Log in to view solution →- A. C1 C6 linkage
- B. C1 C6 linkage
- C. C1 C4 linkage
- D. C1 C4 linkage
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Log in to view solution →- A. 2
- B. 1
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Log in to view solution →- A. Cl
- B. 4 AlCl
- C. AlCl3
- D. Cl+
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Log in to view solution →- A. + 2
- B. + 3
- C. + 4
- D. + 6
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Log in to view solution →- A. 2Ag Ag+ Zn Zn2+
- B. Ag+ Ag Zn2+ Zn
- C. Ag Ag+ Zn Zn2+
- D. Zn Zn2+ Ag+ Ag
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Log in to view solution →- A. positive, negative
- B. negative, negative
- C. negative, positive
- D. positive, positive
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Log in to view solution →- A. H
- B. G
- C. Ea
- D. S
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Log in to view solution →- A. Sucrose
- B. Maltose
- C. Glucose
- D. Lactose
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Log in to view solution →- A. Both Assertion (A) and Reason (R) are true and Reason (R) is the correct explanation of the Assertion (A).
- B. Both Assertion (A) and Reason (R) are true, but Reason (R) is not the correct explanation of the Assertion (A).
- C. Assertion (A) is true, but Reason (R) is false.
- D. Assertion (A) is false, but Reason (R) is true.
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Log in to view solution →- A. Both Assertion (A) and Reason (R) are true and Reason (R) is the correct explanation of the Assertion (A).
- B. Both Assertion (A) and Reason (R) are true, but Reason (R) is not the correct explanation of the Assertion (A).
- C. Assertion (A) is true, but Reason (R) is false.
- D. Assertion (A) is false, but Reason (R) is true.
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Log in to view solution →The rate of reaction is concerned with decrease in concentration of reactants or increase in the concentration of products per unit time. It can be expressed as instantaneous rate at a particular instant of time and average rate over a large interval of time. Mathematical representation of rate of reaction is given by rate law. Rate Constant and order of a reaction can be determined from rate law or its integrated rate equation.
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Log in to view solution →In coordination compounds, metals show two types of linkages, primary and secondary. Primary valencies are ionisable and are satisfied by negatively charged ions. Secondary valencies are non-ionisable and are satisfied by neutral or negative ions having lone pair of electrons. Primary valencies are non-directional while secondary valencies decide the shape of the complexes.
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