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Interpretation:
The structural isomer, chirality and systematic name should be identified for the given formula of
Concept introduction:
Isomer: Molecule has same molecular formula but different structural arrangement is called isomer.
Chiral: Absence of a plane of symmetry or a center of symmetry is called chiral molecule, a non-superimposable on its mirror image is called chiral. A carbon atom is attached by the four different groups is called chiral carbon.
Achiral: Presence of a plane of symmetry or a center of symmetry is called achiral molecule, a superimposable on its mirror image is called achiral. A carbon atom does not have four different groups is called achiral carbon
Geometric isomerism (also known as E-Z isomerism or cis-trans isomerism): same molecular formula but different arrangement in the space. These isomers happen where you have restricted rotation in a molecule (double bond in the molecule). The
Organic compounds are named systematically by using IUPAC rules.
Name of the organic compounds are given according to the number of carbon present in the molecule for example
A molecule having one carbon atom, the molecule name will start with meth etc.…
If any halogens are present in the molecule, the name of the halogens as follows.
Naming the substituted
- (1) Name the parent alkane (long alkyl chain)
- (2) Number the carbon
- (3) Name and number the substituent
If the molecules have the multiple substituents, the compound named as di, tri, tetra, penta, ect.
If the molecules having functional group, the name of the compound is given below. Numbering should be starts from the functional group of the given molecule.
The given compound is an alcohol
Example is given below
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Chapter 11 Solutions
EBK GENERAL CHEMISTRY: THE ESSENTIAL CO
- Nonearrow_forwardDraw a Newman projection from carbon 3 to carbon 2 in the highest energy conformation for the following molecule. What is this conformation called? What kind of strain is present? Brarrow_forwardWhich of the following dienophiles is most reactive in a Diels-Alder reaction: Please explain why the correct answer to this question is option 5. Please provide a detailed explanation.arrow_forward
- Which of the following would you expect to be aromatic? Please provide a detailed explanation.arrow_forwardDraw the enantiomer and diastereomers of the following molecule. Label each type of stereoisomers. Label each chiral center as R or S. HOarrow_forwardWhich diene and dienophile would you choose to synthesize the following compound? Please provide a detailed explanation. Please include a drawing showing the mechanism of the synthesis. Please also explain why it is the correct diene and dienophile.arrow_forward
- Using the sketcher below, draw the structure of N-ethyldecylamine. Answer: 0 ୨୫) . 始 {n [ ]t ?arrow_forwardWhich of the following would you expect to be aromatic? Please provide a detailed explanation.arrow_forwardIdentify the characteristic signals that you would expect in the diagnostic region of an IR spectrum of each of the following compounds. a. H₂N b.arrow_forward
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