Write the bond line formula of the following compounds: (a) 4-methyl-2-hexene, two geometrical (stereoisomers) isomers (b) 3-fluoro-2-methylheptanol (3-fluoro-2-methylheptan-1-ol) (c) 4-methyl-hex-1-yn-3-ol
Introduction to Organic Chemistry
The field of chemistry which deals with the studies of reactions, structures, and properties of organic compounds that comprise carbon bonded through covalent bonding is organic chemistry. The studies regarding the structure of organic compounds could be determined with the help of structural formulas. In order to know about the behavior of organic compounds, a study on the properties has to be done. Both physical properties and chemical properties, the origin of chemical reactivity come under the study regarding the properties of organic compounds. The chemical preparation of polymers, drugs, natural products, and the study of separate organic molecules in the lab come under the study of organic reactions.
Vinyl Group
Vinyl group is the name given to the functional group of -CH=CH2. It can be seen as an ethene molecule with one less hydrogen in number. Hence it is also called as ethenyl group at times.
Straight Chain Hydrocarbons
The requirement to identify each compound needs a richer number of words than informative prefixes like n and iso. The identification of organic molecules is made easier by the use of systematic nomenclature schemes. The organic chemistry nomenclature has two types: traditional and systematic. Common names arise in many forms, but share the characteristic that a link through name and form is unnecessary. The name that matches a certain structure clearly must be remembered as knowing a person's name. In contrast, systemic names, including an overall common set of laws, are locked specifically to the chemical structure.
Unsaturated Hydrocarbon
Following are few examples of alkenes with their general molecular as well as their structural formulas:
Conjugated Compounds in Organic Chemistry
The delocalization of electrons in a molecule is called conjugation in organic chemistry. This delocalisation process of electrons leads to the shortenings or elongations of chemical bonds, but at the same time it causes changes in the chemical properties in conjugated molecules as compared to the non-conjugated ones. For example, conjugated molecules absorb light at longer wavelengths.
Alpha Carbon And Alpha Protons
The carbon directly attached to the functional group in an organic molecule is referred to as the alpha carbon and the hydrogen attached to an alpha carbon are termed as the alpha hydrogens or alpha protons. These alpha carbon atoms and alpha hydrogen atoms are of importance because they undergo certain characteristic reactions in organic chemistry.
Write the bond line formula of the following compounds:
(a) 4-methyl-2-hexene, two geometrical (stereoisomers) isomers
(b) 3-fluoro-2-methylheptanol (3-fluoro-2-methylheptan-1-ol)
(c) 4-methyl-hex-1-yn-3-ol
Here are some key conventions used in bond line structures:
Carbon atoms: Carbon atoms are usually represented by the ends and intersections of lines. Each endpoint or intersection of lines is assumed to be a carbon atom unless otherwise indicated.
Hydrogen atoms: Hydrogen atoms bonded to carbon atoms are not explicitly shown; instead, they are assumed to be present. Typically, chemists assume that carbon atoms are bonded to enough hydrogen atoms to satisfy their valency. For example, a carbon atom with three lines extending from it is assumed to be bonded to three hydrogen atoms.
Other atoms: Atoms other than carbon and hydrogen (e.g., oxygen, nitrogen, sulfur) are typically shown explicitly with their chemical symbols. Their bonds to carbon atoms are represented by lines connecting them to carbon atoms.
Double and triple bonds: Double bonds are represented by two parallel lines (=) between two carbon atoms, while triple bonds are represented by three parallel lines (≡).
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