Question:medium

What are the oxidation numbers of the underlined elements in each of the following and how do you rationalise your results? 
(a) KI3 (b) H2S4O6 (c) Fe3O4 (d) CH3CH2OH (e) CH3COOH

Updated On: Jan 19, 2026
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Solution and Explanation

(a) KI₃

Formula is better written as K^+[I3]^-; the underlined element is iodine in ce{I3^-.

Let oxidation number of each I in \(\ce{I3^-}\) be \(x\): \[ 3x = -1 \Rightarrow x = -\frac{1}{3} \]

Result: Oxidation number of I in \(\ce{I3^-}\) is \(-\dfrac{1}{3}\). This fractional value arises because \(\ce{I3^-}\) is a resonance-stabilised polyiodide ion with delocalised charge over three equivalent I atoms.

(b) H₂S₄O₆ (tetrathionic acid)

Underlined element: S.

Assign usual oxidation numbers: \[ 2(+1) + 4(x) + 6(-2) = 0 \] \[ 2 + 4x - 12 = 0 \Rightarrow 4x - 10 = 0 \Rightarrow x = +\frac{10}{4} = +2.5 \]

Average oxidation state of S in \(\ce{H2S4O6}\) is \(+2.5\).

Structurally, tetrathionic acid contains sulphur atoms in different environments (some at higher, some at lower oxidation states), and their average comes out as +2.5.

(c) Fe₃O₄

Underlined element: Fe.

\(\ce{Fe3O4}\) is a mixed oxide often written as \(\ce{FeO·Fe2O3}\), containing both Fe(II) and Fe(III).

Let the average oxidation state of Fe be \(x\): \[ 3x + 4(-2) = 0 \Rightarrow 3x - 8 = 0 \Rightarrow x = +\frac{8}{3} \]

Result: Average oxidation number of Fe is \(+\dfrac{8}{3}\), rationalised as 1 Fe in +2 state and 2 Fe in +3 state: \[ \frac{(+2) + 2(+3)}{3} = \frac{8}{3}. \]

(d) CH₃CH₂OH (ethanol)

There are two different carbons; usually the question underlines one specific C. Give oxidation numbers of both C atoms for clarity.

  • Let oxidation state of first carbon (C₁ in CH₃–) be \(x_1\), of second carbon (C₂ in –CH₂OH) be \(x_2\).
  • Assign usual values: H = +1, O = –2.

For C₁ in CH₃– (bonded to 3 H and 1 C): Count using whole molecule approach: Total for molecule: \[ x_1 + x_2 + 6(+1) + (-2) = 0 \Rightarrow x_1 + x_2 + 4 = 0 \]

For C₂ in –CH₂OH (one C, two H, one O, one H): Oxidation number around this carbon: \[ x_2 + 2(+1) + (-2) + (+1) = 0 \Rightarrow x_2 + 1 = 0 \Rightarrow x_2 = -1 \] Put in total equation: \[ x_1 + (-1) + 4 = 0 \Rightarrow x_1 + 3 = 0 \Rightarrow x_1 = -3 \]

Result: In \(\ce{CH3CH2OH}\): C in \(\ce{CH3-}\): –3; C in \(\ce{-CH2OH}\): –1. The carbon bonded to more electronegative O is less reduced (–1) than the terminal methyl carbon (–3).

(e) CH₃COOH (acetic acid)

Again, two distinct carbons.

  • C₁ in \(\ce{CH3-}\)
  • C₂ in \(\ce{-COOH}\) (the carboxyl carbon)

For C₂ in –COOH group:

Consider the –COOH part: \(\ce{CO2H}\). Let oxidation number of that carbon be \(x_2\): \[ x_2 + 2(-2) + (+1) = 0 \Rightarrow x_2 - 4 + 1 = 0 \Rightarrow x_2 = +3 \]

For C₁ in CH₃– (same logic as in alkane methyl group): Treat the bond to C₂ as to an atom of similar electronegativity, so: \[ x_1 + 3(+1) = 0 \Rightarrow x_1 = -3 \]

Result: In \(\ce{CH3COOH}\): methyl carbon (C₁) = –3, carboxyl carbon (C₂) = +3. This illustrates that within one molecule, different atoms of the same element can have very different oxidation states, and an average value would not reflect their actual redox character.

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