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Enter the degree of unsaturation for the molecule below.

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Final answer:

The degree of unsaturation, also known as the index of hydrogen deficiency (IHD), determines the number of pi bonds and/or rings in a molecule based on its deviation from the saturated alkane formula. It is calculated using a formula that accounts for the number of carbons, hydrogens, halogens, oxygens, and nitrogens in the molecule.

Step-by-step explanation:

The degree of unsaturation (DOU), also known as the index of hydrogen deficiency (IHD), is a calculation used in organic chemistry to determine the number of rings and/or multiple bonds in a molecule. The general formula of an alkane is CnH(2n+2), and each degree of unsaturation represents a deviation of two hydrogen atoms from this formula.

This deviation could be because of a ring or a double bond, which both reduce the hydrogen count by two per unsaturation degree. Additional factors such as the presence of halogens, oxygen, or nitrogen atoms affect the hydrogen count differently. Halogens (X) are counted as hydrogen atoms since they replace hydrogen in the molecule, oxygen (O) does not alter hydrogen count, and nitrogen (N) add one hydrogen. Therefore, to calculate the IHD, we use the following formula:

(2C + 2 + N - X - H)/2

Where C is the number of carbon atoms, N is the number of nitrogen atoms, X is the number of halogen atoms, and H is the number of hydrogen atoms. This formula will give you the total degree of unsaturation, indicating the total number of rings and/or pi bonds (double or triple bonds) in the molecule.

Alkenes are unsaturated hydrocarbons with one or more double bonds, and alkynes have one or more triple bonds. These bonds affect the molecule's geometry, leading to differences in molecular shape and properties compared to saturated counterparts that lack these bonds. For example, a molecule with a single double bond will have an IHD of 1, indicating it is an alkene.

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