An IUPAC name has to be assigned to Myristic acid. Concept introduction: The length of the carbon chain and the degree of unsaturation in the fatty acid helps in assigning an IUPAC name to a fatty acid. The carbon chain may or may not contain carbon-carbon double bonds. The naming of straight chain alkanes is done on the basis of number of carbon atoms present in the longest carbon chain.
An IUPAC name has to be assigned to Myristic acid. Concept introduction: The length of the carbon chain and the degree of unsaturation in the fatty acid helps in assigning an IUPAC name to a fatty acid. The carbon chain may or may not contain carbon-carbon double bonds. The naming of straight chain alkanes is done on the basis of number of carbon atoms present in the longest carbon chain.
Solution Summary: The author explains that an IUPAC name has to be assigned to Myristic acid. The naming of straight chain alkanes is done on the basis of number of carbon atoms present in the longest carbon chain
Definition Definition Group of atoms that shape the chemical characteristics of a molecule. The behavior of a functional group is uniform in undergoing comparable chemical reactions, regardless of the other constituents of the molecule. Functional groups aid in the classification and anticipation of reactivity of organic molecules.
Chapter 19, Problem 19.19EP
(a)
Interpretation Introduction
Interpretation: An IUPAC name has to be assigned to Myristic acid.
Concept introduction: The length of the carbon chain and the degree of unsaturation in the fatty acid helps in assigning an IUPAC name to a fatty acid. The carbon chain may or may not contain carbon-carbon double bonds. The naming of straight chain alkanes is done on the basis of number of carbon atoms present in the longest carbon chain.
(b)
Interpretation Introduction
Interpretation: An IUPAC name has to be assigned to Palmitoleic acid.
Concept introduction: The length of the carbon chain and the degree of unsaturation in the fatty acid helps in assigning an IUPAC name to a fatty acid. The carbon chain may or may not contain carbon-carbon double bonds. The naming of straight chain alkenes is similar to alkanes except that the suffix changes to “-ene”.
Draw the Fischer projection from the skeletal
structure shown below.
HO
OH
OH
OH
OH H
Q
Drawing
Atoms, Bonds
and Rings
Charges
I
☐
T
HO
H
H
OH
HO
I
CH2OH
H
OH
Drag
H
OH
-CH2OH
CHO
-COOH
Undo
Reset
Remove
Done
please provide the structure for this problem, thank you
presented by Morallen Lig
Intermine the hand product for the given mution by adding atoms, bonds, nonhonding diarion panda
скуль
Step 3: Comp the draw the product
Step 2: Agama workup Compithe
429
ملولة
Chapter 19 Solutions
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