ORGANIC CHEMISTRY,SOLN.MAN.+...-ACCESS
ORGANIC CHEMISTRY,SOLN.MAN.+...-ACCESS
4th Edition
ISBN: 9781119659471
Author: Klein
Publisher: WILEY
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Chapter 1.6, Problem 6LTS
Interpretation Introduction

Interpretation: The number of carbon atoms present in diazepam should be identified and all the hydrogen atoms needs to be filled in the structure.

Concept Introduction: A method used to represent molecular structures of compounds is said to be bond line notation. In this notation, a line depicts a bond between two atoms and are drawn in a zigzag format. Atoms other than carbon and hydrogens are specifically depicted in this notation. It is assumed that carbon atoms are bonded to enough hydrogen atoms that are required to complete the octet.

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Functional Groups FUNCTIONAL GROUPS IN ORGANIC CHEMISTRY FUNCTIONAL GROUPS ARE GROUPS OF ATOMS IN ORGANIC MOLECULES THAT ARE RESPONSIBLE FOR THE CHARACTERISTIC CHEMICAL REACTIONS OF THOSE MOLECULES. IN THE GENERAL FORMULAE SHOWN BELOW FOR EACH FUNCTIONAL GROUP, 'R' REPRESENTS THE REST OF THE MOLECULE, AND X REPRESENTS ANY HALOGEN ATOM. HALOGEN HETEROATOMICS CARBONYL COMPOUNDS HYDROCARBONS SIMPLE OXYGEN HETEROATOMICS NITROGEN-BASED SULFUR-BASED AROMATIC R-OH 0-R₂ R-X ALKANE ALKENE ALKYNE EPOXIDE Noming one egethane Noming ene egethene Noming ye ALCOHOL Naming-of egethanol ETHER Naming-ory ane eg. methoxyethane Naming ene oxide egethene oxide HALOALKANE Naming: holo eg. chloroethane eg ethyne ÅR (PNP) -Å-X OR₂ ALDEHYDE Naming al eg ethanal KETONE Naming: one eg propanone CARBOXYLIC ACID Naming oic acid eg, ethanoic acid ACID ANHYDRIDE Noming oic anhydride eg. ethanoic anhydride ESTER Naming late eg. ethyl ethanoate AMIDE Naming: amide eg. ethanamide ACYL HALIDE Naming ay halide eg…
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TRUE OR FALSE All atoms play a role in the physicochemical and pharmacologic properties of a molecule. Sophistication and advancement in technology are the main driving forces of drug development. Organic medicinal chemistry is the study of matter, specifically, all carbon-containing compounds. A functional group will always have the same physicochemical properties, regardless of its neighboring atoms in a molecular structure. Addition of a single methyl group in a drug molecule may result to changes in physical, chemical, pharmacokinetic, and pharmacologic properties. Steric effects occur when bulky and large functional groups are near each other in a molecular structure. Molecules that are highly capable of hydrogen bonding tend to be more soluble in nonpolar solvents.
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