The OH peaks in the IR spectra of benzyl alcohol and benzoic acid should be compared and contrasted.
<h3>What is the IR spectra of Benzoic acid?</h3>
- The right-hand portion of the infrared spectrum of benzoic acid, between wavenumbers 1500 and 400 cm-1, is referred to as the fingerprint region.
- It results from a special combination of intricately overlapping vibrations of the atoms within the benzoic acid molecule.
<h3>What is the IR spectra of Benzyl alcohol?</h3>
- A C-Cl bond is frequently shown by a peak at 700.
- There are a few more peaks at 1500 that are directed at a C=C bond.
<h3>What is IR spectra?</h3>
The percent transmittance (or absorbance) of the radiation through the molecule against the radiation's wave number forms the IR spectrum.
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Answer:
option C= 12.40
Explanation:
Formula:
pH + pOH = 14
First of all we will calculate the pH.
pH = - log [H⁺]
pH = - log [0.025]
pH = - (-1.6)
pH = 1.6
Now we will put the values in formula,
pH + pOH = 14
pOH = 14-pH
pOH = 14 -1.6
pOH = 12.4
The pOH of solution is 12.4.
The ions of Noble gases, <em>group VIII</em> elements have a full octet configuration on their outermost shell and as such are highly stable.
The periodic table is a systematic arrangement of elements in order of their atomic numbers into a set of 8 columns each called groups and a set of 7 rows each called a period.
Elements are arranged in different groups according to the number of Valence electrons they have.
- For instance, elements in the group I of the periodic table are highly electropositive and as such are highly reactive.
The same is evident in group 7 elements are highly electronegative and have high electron affinity and as such are unstable and reactive.
- However, Noble gases, <em>group VIII</em> elements have a full octet configuration on their outermost shell and as such are highly stable.
Consequently, the <em>Noble gases ion</em> has a stable Valence electron configuration.
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Argon has 24 known isotopes.
Its inorganic as MgCO3 is contains no carbon more hydrogen which is a crutial component of all organic compounds
