Degree of unsaturation why is it 5?

C20H32CIN
do i ignore the second C?
because i did
21(2)+2=44 44-32+1-1 / 2 = 6
but i get it right with
20(2)+2=42 42-32-1+1 / 2 = 5
do i always ignore extra C's?

No, you don't ignore a second C; all should be counted. I don't think that is a C. I think it is a Cl (chlorine).

So you have
20C
32H
1Cl
1N which gives you
[2+2(20)-32+1-1]/2 = 5
Viola!

you're right! sorry i guess im just tired from over studying that i saw the wrong letter!

The degree of unsaturation is calculated based on the molecular formula and provides information about the presence of multiple bonds or rings in a compound. It helps in determining the structure and properties of the compound.

In your example, the molecular formula is C20H32ClN. To calculate the degree of unsaturation, you need to consider the number of hydrogen atoms present and adjust for any additional elements like chlorine (Cl) in this case.

Now, let's break it down step-by-step:

1. Write out the molecular formula: C20H32ClN.

2. Calculate the number of hydrogens: 20 carbons would have 40 hydrogen atoms, and nitrogen (N) typically has 3 hydrogen atoms bonded to it.

3. Add up the total number of hydrogens: 40 (from the carbons) + 32 (from the hydrogens) + 3 (from the nitrogen) = 75.

4. Adjust for the chlorine atom: Since chlorine doesn't contribute any hydrogens, subtract 1.

5. Calculate the degree of unsaturation: The formula is given by (2C + 2 + N - H)/2.

Using the adjusted values, it becomes (2(20) + 2 + 1 - 75)/2:
(40 + 2 + 1 - 75)/2 = -32.

The negative value indicates that there is no degree of unsaturation.

In summary, for the given compound C20H32ClN, the correct calculation for the degree of unsaturation is 0, meaning there are no multiple bonds or rings present.

Regarding your question about ignoring extra carbon atoms, please note that it is important to consider all elements present in the molecular formula when calculating the degree of unsaturation, including any additional carbon atoms.

The degree of unsaturation, also referred to as the index of hydrogen deficiency (IHD), is a calculation used to determine the level of unsaturation (double bonds or rings) in a molecular formula. It provides information about the structural features of a compound.

To calculate the degree of unsaturation, you can use the formula (2n + 2) - H - (X/2), where 'n' represents the number of carbons, 'H' is the number of hydrogens, and 'X' is the number of halogens, nitrogen, or oxygen atoms.

Let's analyze the molecular formula C20H32ClN to calculate the degree of unsaturation using the formula:

- First, determine the number of carbons (C). In this case, it is 20.
- Next, calculate the number of hydrogens (H). The formula implies that each carbon should have 2 hydrogens except for terminal carbons, which have 3 hydrogens. So, 20 carbons would have (20 * 2) + 2 hydrogens, which equals 42 hydrogens.
- Additionally, check if there are any halogens, nitrogen, or oxygen atoms present. In this formula, there is one chlorine atom (Cl).
- Substituting these values into the formula, (2n + 2) - H - (X/2) becomes (2 * 20) + 2 - 42 - (1/2).
- Simplifying this expression, (40 + 2) - 42 - 0.5 = 44 - 42 - 0.5 = 1.5.

Based on this calculation, the degree of unsaturation for C20H32ClN is 1.5. However, since the degree of unsaturation should be a whole number, you can round it down to 1.

Regarding your question about ignoring additional carbon atoms, the formula for degree of unsaturation assumes that all carbons are accounted for in the molecular formula. It does not involve selectively ignoring any carbon atoms. Therefore, it is essential to include all carbon atoms when calculating the degree of unsaturation.

In the case of your second example, C20H32, when you correctly accounted for all the atoms and used the formula (2n + 2) - H - (X/2), you obtained a degree of unsaturation of 5. This result is accurate since all the carbon atoms are considered.

Remember to double-check your calculations and ensure that you include all relevant atoms in the molecular formula to accurately calculate the degree of unsaturation.