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”.
Calculate activation energy (Ea) from the following kinetic data: Temp (oC) Time (s) 23.0 180. 32.1 131 40.0 101 51.8 86.0 Group of answer choices 0.0269 kJ/mole 2610 kJ/mole 27.6 kJ/mole 0.215 kJ/mole 20.8 kJ/mole
Calculate activation energy (Ea) from the following kinetic data: Temp (oC) Time (s) 23.0 180. 32.1 131 40.0 101 51.8 86.0 choices: 0.0269 kJ/mole 2610 kJ/mole 27.6 kJ/mole 0.215 kJ/mole 20.8 kJ/mole
Calculate activation energy (Ea) from the following kinetic data:
Temp (oC) Time (s)
23.0 180.
32.1 131
40.0 101
51.8 86.0
Chapter 19 Solutions
Study Guide with Selected Solutions for Stoker's General, Organic, and Biological Chemistry, 7th
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