<u>Ionic Bond</u> is formed when the electronegativity difference is 0.4 > 2.0. Electronegativity is a term that can be defined as a tendency of an atom to attract electron towards its own self.
Explanation:
Electronegativity is a term that can be defined as a tendency of an atom to attract electron towards its own self.
An electronegativity of an atom is affected by
- The atomic number of the atom
- Secondly by the distance at which the valence electron are residing from the nucleus
1. In case the electronegativity difference (which is denoted by ΔEN) is less than 0.5 then the bond formed is known as N<u>onpolar covalent.
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2. In case the ΔEN is in between 0.5 and 1.6, the bond formed is referred to as the<u> Polar covalent
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3. In case the ΔEN is more /greater than 2.0, then the bond formed is referred to as<u> Ionic Bond</u>
<u>2 Examples of Ionic bonds</u>
- The formation of sodium fluoride, NaF, from a sodium atom and a fluorine atom is an example of Ionic bond formation.
- Another example is the formation of NaCl from sodium (Na),which is a metal, and chloride (Cl), which is a nonmetal
1.6726219 × 10-27 kilograms
(The -27 is a exponent)
Answer:p-hydroxybenzaldehyde is stronger acid to phenol
para-cyanophenol is stronger acid to meta-cyanophenol
o-fluorophenol is stronger acid to p-fluorophenol.
Explanation:
The PKa tool relative to Ph are used to contrast the pairs.
The pKa of phenol is 10. The pKa of p-hydroxybenzaldehyde is 9.24
The pKa for meta-cyanophenol is 8.61 and the pKa for para-cyanophenol is 7.95.
The pKa value of o-fluorophenol is 8.7, while that of the p-fluorophenol is 9.9. It's obvious that the inductive effect is more dominant at ortho-position, which results in a more acidic nature
The pKa is the pH value at which a chemical species will accept or donate a proton. The lower the pKa, the stronger the acid and the greater the ability to donate a proton in aqueous solution.
No polysaccharides are complex forms of carbohydrate of long sugar molecules
