- A. Iron (Z = 26)
- B. Manganese (Z = 25)
- C. Chromium (Z = 24)
- D. Vanadium (Z = 23)
The electronic configuration of Manganese (Mn, Z=25) is [Ar] 3d5 4s2. Removing two electrons (first and second ionization) leaves the stable half-filled 3d5 configuration. The third ionization involves removing an electron from this stable half-filled d-subshell, which requires significantly higher energy compared to the other elements listed, where the d-subshell is not half-filled or is more easily ionized.
- A. (CH3)2CH CH2OH
- B. CH3CH2CH2OH
- C. (CH3)3C OH
- D. CH3 CH2 CH CH3 | OH
Chromic anhydride (CrO3) in acidic medium is a strong oxidizing agent. Secondary alcohols are oxidized to ketones. (CH3)2CHCH2OH (primary) forms an aldehyde then acid; CH3CH2CH2OH (primary) forms an aldehyde then acid; (CH3)3COH (tertiary) is generally resistant to oxidation under these conditions; CH3CH2CH(OH)CH3 is a secondary alcohol, which undergoes oxidation to form butanone (a ketone).
- A. Adenine
- B. Phosphoric acid
- C. Sulphuric acid
- D. Uracil
The three components of a nucleotide (which makes up DNA) are a nitrogenous base (like Adenine, Guanine, Cytosine, or Thymine), a pentose sugar (2-deoxyribose in DNA), and a phosphate group (derived from phosphoric acid).
- A. is always greater than one
- B. has negative value
- C. has zero value
- D. is always less than one
The van't Hoff factor (i) is defined as the ratio of observed colligative property to calculated colligative property. When a solute undergoes association, the number of particles in the solution decreases, causing the value of i to be less than one.
- A. 2d P d Y = dt dt
- B. d P d X = dt dt
- C. + d X d P = dt dt
- D. 2d Y + d P = dt dt
For the reaction X + 2Y -> P, the rate of reaction is given by -d[X]/dt = -(1/2)d[Y]/dt = +d[P]/dt. Rearranging the terms related to X and P, we get -d[X]/dt = d[P]/dt.
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Log in to view solution →- A. Cl CH2 COCl
- B. Cl CH2 COOH
- C. CH3 COCl
- D. CCl3 COOH
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Log in to view solution →- A. nucleophilic addition
- B. electrophilic addition
- C. nucleophilic substitution
- D. electrophilic substitution
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Log in to view solution →- A. slope is A/R and intercept is Ea.
- B. slope is A and intercept is Ea/R.
- C. slope is Ea/RT and intercept is log A.
- D. slope is 2·303 R/Ea and intercept is log A.
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Log in to view solution →- A. Wurtz reaction
- B. Reimer-Tiemann reaction
- C. Williamson synthesis
- D. Kolbe reaction
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Log in to view solution →- A. (CH3)3C OH > (CH3)2CH OH > CH3CH2 OH
- B. (CH3)2CH OH > CH3CH2 OH > (CH3)3C OH
- C. CH3CH2 OH > (CH3)2CH OH > (CH3)3C OH
- D. (CH3)2CH OH > (CH3)3C OH > CH3CH2 OH
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Log in to view solution →- A. Aldehyde group and hydroxyl group at C 4
- B. Aldehyde group and hydroxyl group at C 5
- C. Ketone group and hydroxyl group at C 4
- D. Ketone group and hydroxyl group at C 5
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Log in to view solution →- A. (i) CH3 CH = CH Br
- B. (ii) CH2 = CH CH CH3 | Br
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Log in to view solution →29. Batteries and fuel cells are very useful forms of galvanic cell. Any battery or cell that we use as a source of electrical energy is basically a galvanic cell. However, for a battery to be of practical use it should be reasonably light, compact and its voltage should not vary appreciably during its use. There are mainly two types of batteries primary batteries and secondary batteries. In the primary batteries, the reaction occurs only once and after use over a period of time the battery becomes dead and cannot be reused again, whereas the secondary batteries are rechargeable. Production of electricity by thermal plants is not a very efficient method and is a major source of pollution. To solve this problem, galvanic cells are designed in such a way that energy of combustion of fuels is directly converted into electrical energy, and these are known as fuel cells. One such fuel cell was used in the Apollo space programme.
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Log in to view solution →30. The Valence Bond Theory (VBT) explains the formation, magnetic behaviour and geometrical shapes of coordination compounds whereas for coordination compounds is based on the effect of different crystal fields (provided by ligands taken as point charges), on the degeneracy of d-orbital energies of the central metal atom/ion. The splitting of the d-orbitals provides different electronic arrangements in strong and weak crystal fields. The crystal field theory attributes the colour of the coordination compounds to d-d transition of the electron. Coordination compounds find extensive applications in metallurgical processes, analytical and medicinal chemistry.
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Log in to view solution →The Valence Bond Theory (VBT) explains the formation, magnetic behaviour and geometrical shapes of coordination compounds whereas for coordination compounds is based on the effect of different crystal fields (provided by ligands taken as point charges), on the degeneracy of d-orbital energies of the central metal atom/ion. The splitting of the d-orbitals provides different electronic arrangements in strong and weak crystal fields. The crystal field theory attributes the colour of the coordination compounds to d-d transition of the electron. Coordination compounds find extensive applications in metallurgical processes, analytical and medicinal chemistry.
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