How could you distinguish between cyclohexane and cyclohexene using ir?

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When we are performing IR spectroscopy for Cyclohexane and cyclohexene, we can distinguish them as cyclohexene has C-H carbon-hydrogen stretching so, it shows the absorption at 3000-2850 cm⁻¹ range, where the cyclohexane do not have this and it shows the -C=C- stretch at 1640-1680 cm⁻¹ range in the spectrum. So that is how we can distinguish both.

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There are two binary compounds of mercury and oxygen. heating either of them results in the decomposition of the compound, with

grandymaker [24]

$\text{Hg} \text{O}$ and $\text{Hg}_{2} \text{O}$ .

Assuming complete decomposition of both samples,

$m(\text{Hg}) = m(\text{residure})$
$m(\text{O}) = m(\text{loss})$

First compound:

$m(\text{O}) = m(\text{loss}) = 0.6498 - 0.6018 = 0.048 \; g$
$m(\text{Hg}) = m(\text{residure}) = 0.6018 \; g$

$n = m/M$ ; $0.6498 \; g$ of the first compound would contain

$n(\text{O atoms}) = 0.048 \; g / 16 \; g \cdot mol^{-1}= 0.003 \; mol$
$n(\text{Hg atoms}) = 0.6018 \; g / 200.58 \; g \cdot mol^{-1}= 0.003 \; mol$

Oxygen and mercury atoms seemingly exist in the first compound at a $1:1$ ratio; thus the empirical formula for this compound would be $\text{Hg} \text{O}$ where the subscript "1" is omitted.