ORGANIC CHEMISTRY (LL)-PACKAGE
ORGANIC CHEMISTRY (LL)-PACKAGE
8th Edition
ISBN: 9781319316389
Author: VOLLHARDT
Publisher: MAC HIGHER
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Chapter 1, Problem 54P
Interpretation Introduction

Interpretation: The molecular formulaof compound that has 84% carbon should be chosen.

Concept introduction:An empirical formula gives the simplest whole number ratio of atoms of each element present in a molecule. The molecular formula tells the exact number of atoms of each element present in a molecule.

The steps to determine the empirical formula of a compound are as follows:

Divide mass of element by its molar mass to convert mass to moles as follows:

  Amount(mol)=(Given mass(g))(1 molNo. of grams)

The number of moles thus calculated are written as the subscript of the element’s symbol and this results in a preliminary formula for the compound.

In order to convert the moles to the whole number subscripts, each subscript is divided by the smallest subscript.

The sum of the product of the molar mass of each element times number of corresponding atoms results in empirical formula mass.

The formula to calculate the whole number multiple is as follows:

  Wholenumber multiple=Molar mass of compoundEmpirical formula mass

The product of this the whole number with the subscript of each element results in molecular formula.

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Transmitance 3. Which one of the following compounds corresponds to this IR spectrum? Point out the absorption band(s) that helped you decide. OH H3C OH H₂C CH3 H3C CH3 H3C INFRARED SPECTRUM 0.8- 0.6 0.4- 0.2 3000 2000 1000 Wavenumber (cm-1) 4. Consider this compound: H3C On the structure above, label the different types of H's as A, B, C, etc. In table form, list the labeled signals, and for each one state the number of hydrogens, their shifts, and the splitting you would observe for these hydrogens in the ¹H NMR spectrum. Label # of hydrogens splitting Shift (2)
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