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Camphor, a saturated monoketone from the Asian camphor tree, is used among other things as a moth repellent and as a constituent of embalmingfluid. If camphor has M+=152.1201 by high-resolution mass spectrometry,what is its molecular formula? How many rings does camphor have?

Short Answer

Expert verified

The actual formula for camphor is C10H16O(M+=152.1201)corresponding to three degrees of unsaturation. Camphor have two rings.

Step by step solution

01

Step-by-step Solution Step 1: Nitrogen rule

According to nitrogen rule an organic compound having odd molar mass contain odd number of nitrogen atoms and compound having even molar mass contain even number of nitrogen atoms.

02

Calculating Molecular mass of camphor

High resolution mass spectrometry calculate exact mass of the fragments upto 5 ppm level.

We have given M+=152.1201

Consider mass of camphor is 152.

Thus given mass is even it means camphor molecule contain zero or even number of nitrogen atoms, according to nitrogen rule.

According to rule of 13, divide 152 by 13

15213=1311152−143_9

The remainder is 9. The basic C-H formula is: CnH(n+r)

Here n=11 and r=9

C11H(11+9)=C11H20

(n= quotient, r=remainder)

As we know camphor is monoketone, it contain one carbonyl oxygen and so make addition of that oxygen to above CH formula by replacing with CH4.

So, the molecular formula becomes: C11H20−CH4+O=C10H16O

03

Determining rings of camphor by Double Bond equivalent (DBE)

Degree of unsaturation is also known as double bond equivalent (DBE). If molecular formula is given plug in the number into these formula.

DBE=2C+2+N−X−H2

Where, C is the number of Carbons

N is the number of nitrogen’s

H is the number of hydrogens

X is the number of halogens

For C10H16O(M+=152.1201)

DBE=2(10)+2+0−X−162=62=3

The actual formula, C10H16O(M+=152.1201)corresponds to three degree of unsaturation. The ketone functional group accounts for one of these. Since camphor is a saturated compound, the other two degree of unsaturation are due to two rings. Hence, the camphor containing two rings.

Camphor

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Most popular questions from this chapter

Although the Diels–Alder reaction generally occurs between an electron rich diene and an electron-deficient dienophile, it is also possible to

have inverse-demand Diels–Alder reactions between suitable electrondeficient

conjugated double bonds and electron-rich alkenes. These reactions are particularly useful because they allow for the incorporation of heteroatoms into the new six-membered ring. Predict the products of each inverse-demand Diels–Alder reaction below. Be sure your products reflect the correct stereochemistry. If more than one region isomer is possible, draw both.

(a)

(b)

(c)

What are the masses of the charged fragments produced in the following cleavage pathways?

(a)Alpha cleavage of 2-pentanone (CH3COCH2CH2CH3)

(b) Dehydration of cyclohexanol (hydroxy cyclohexane)

(c) McLafferty rearrangement of 4-methyl-2-pentanone [CH3COCH2CH(CH3)2]

(d) Alpha cleavage of triethylamine [(CH3CH2)3N]

Assume that you are carrying out the dehydration of 1-methyl cyclohexanol to yield 1-methyl cyclohexene. How could you use infrared spectroscopy to determine when the reaction is complete?


Assuming that strong acids add to alkynes in the same manner as they add to alkenes, propose a mechanism for each of the following reactions:

Question: Write molecular formulas for compounds that show the following molecular ions in their high-resolution mass spectra, assuming that C, H, N, and O might be present. The exact atomic masses are: 1.00783 (H1), 12.00000 (C12), 14.00307 (N14), 15.99491 (O16).

a)M+=98.0844b)M+=123.0320

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