- A. 1s^2 2s^2 2p^6 3s^2 3p^2
- B. 1s^2 2s^2 2p^4
- C. 1s^2 2s^2 2p^6 3s^2 3p^3
- D. 1s^2 2s^2 2p^3
Elements in group 15 have the valence shell configuration $ns^2 np^3$. The 3rd period indicates the principal quantum number $n=3$. Therefore, the valence shell configuration is $3s^2 3p^3$. Adding the core electrons ($1s^2 2s^2 2p^6$), the full configuration is $1s^2 2s^2 2p^6 3s^2 3p^3$. Choice (A) corresponds to Silicon (Group 14), (B) is Oxygen (Period 2), and (D) is Nitrogen (Period 2).
- A. Al_2O_3 · nH_2O
- B. Fe_2O_3 · 2H_2O
- C. Al_2O_3
- D. None of the above
Bauxite is the principal ore of aluminium and is represented by the formula $Al_2O_3 \cdot nH_2O$. It typically contains varying amounts of water. $Al_2O_3$ (anhydrous) is Corundum, and $Fe_2O_3 \cdot nH_2O$ is Limonite.
- A. 35 minutes
- B. 20 minutes
- C. 75 minutes
- D. 30 minutes
For a first-order reaction, the rate constant $k = \frac{2.303}{t} \log(\frac{[A]_0}{[A]_t})$. When 75% is completed, $[A]_t = 0.25[A]_0$, so $k = \frac{2.303}{60} \log(4) = \frac{2.303}{60} \times 0.602$. The half-life $t_{1/2} = \frac{0.693}{k}$. Substituting $k$, we get $t_{1/2} = \frac{0.693 \times 60}{2.303 \times 0.602} \approx 30$ minutes.
- A. ZnHg/NaOH
- B. Zn/NH_4Cl
- C. Sn/HCl
- D. All of these
Nitrobenzene can be reduced to aniline (amino benzene) using metal-acid combinations like $Sn/HCl$, $Fe/HCl$, or $Zn/HCl$ (catalytic hydrogenation is also possible). $Sn/HCl$ is the standard laboratory method. $Zn/NH_4Cl$ is typically used to stop at the intermediate phenylhydroxylamine stage, and $ZnHg/NaOH$ is a Clemmensen reduction condition usually reserved for carbonyls.
- A. Methanal
- B. Methanoic acid
- C. CO_2
- D. Glyoxal
Periodic acid ($HIO_4$) cleaves 1,2-diols (vicinal diols) at the C-C bond. For ethylene glycol ($HO-CH_2-CH_2-OH$), the cleavage results in two molecules of formaldehyde ($CH_2O$ or methanal).
- A. K_4[Fe(CN)_6]
- B. [Fe(CN)_3(NH_3)_3]
- C. [Fe(CO)_5]
- D. Both (b) and (c)
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Log in to view solution →- A. HPO_4^{2-}
- B. HCl
- C. Br^-
- D. SO_4^{2-}
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Log in to view solution →- A. basic
- B. neutral
- C. amphoteric
- D. acidic
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Log in to view solution →- A. Hydrogenation of oil
- B. Manufacture of ammonia by Haber’s process
- C. Hydrolysis of sucrose in presence of dil.HCl
- D. Manufacture of sulphuric acid by Contact process
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Log in to view solution →- A. electrophilic addition
- B. nucleophilic substitution
- C. nucleophilic addition
- D. electrophilic substitution
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Log in to view solution →- A. 15
- B. 14
- C. 13
- D. 12
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Log in to view solution →- A. Charge required to deposit one mole of substance
- B. Charge carried by 1 electron
- C. Charge carried by 6.22 \times 10^{10} electrons
- D. Charge carried by one mole of electrons
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Log in to view solution →- A. Proline
- B. Alanine
- C. Glycine
- D. Leucine
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Log in to view solution →- A. ZnO
- B. NaCl
- C. KCl
- D. FeO
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Log in to view solution →- A. liquid in gas
- B. solid in gas
- C. gas in liquid
- D. gas in gas
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