
Concept explainers
Interpretation:
The correct option among the given options has to be chosen.
Concept Introduction:
Organic compounds are represented shortly by the molecular formula and structural formula. Each and every compound has its own molecular formula. Compounds can have same molecular formula but not same structural formula.
Isomers are the compounds that have same molecular formula but different structural formula. The main difference lies in the way the atoms are arranged in the structure. Isomers have different chemical and physical properties even when they have same molecular formula. This is known as Isomerism.
If there is difference only in the connectivity of the atoms in the molecule, then it is known as constitutional isomerism. The isomers are known as constitutional isomers. They will have same molecular formula and same
For constitutional isomers to be present in cycloalkane, a minimum of four carbon atoms has to be present.
Cycloalkanes can also exhibit stereoisomerism. The difference between constitutional isomerism and stereoisomerism is that, the result of difference in connectivity of carbon atoms is known as constitutional isomerism and the result of differences in configuration is known as stereoisomerism. Stereoisomers are compounds that possess same molecular formula and connectivity of atoms but different orientations of atoms in space. Cis isomers are the one where the two substituted groups on different carbon atom are present above or below the plane or the ring of carbon atoms. Trans isomers are the one where the two substituted groups on different carbon atom are present one above and one below the plane or the ring of carbon atoms.

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Chapter 12 Solutions
General, Organic, and Biological Chemistry
- no Ai walkthroughsarrow_forward136 PRACTICAL SPECTROSCOPY Compound 78 is a high-boiling liquid (boiling point 189° C) that contains halogen, but will not react with alkoxides to yield an halogen. ether. The Mass, IR, and 'H NMR spectra, along with 13C NMR data, are given below. Elemental Analysis: C, 35.32; H, 2.47; contains BC Spectral Data: doublet, 137.4 ppm; doublet, 130.1 ppm; doublet, 127.4 ppm; singlet, 97.3 ppm Absorbance Mass Spectrum Intensity 77 77 204 M + 128 40 60 80 100 120 140 160 180 m/e 200 220 280 240 260 300 Infrared Spectrum Wave Number, cm -1 4000 3000 2500 2000 1500 1300 1200 1100 1000 900 800 700 3 6 7 8 9 10 12 13 15 Wavelength, microns 'H NMR wwwww 5 Structure: www ppm, & ©2000 Brooks/Cole Publishing Com-arrow_forwardno Ai walkthroughsarrow_forward
- 3. Synthesize the following synthon from the indicated starting material. i HO.arrow_forwardIdentifying the stereochemistry of natural Write the complete common (not IUPAC) name of each molecule below. Note: if a molecule is one of a pair of enantiomers, be sure you start its name with D- or L- so we know which enantiomer it is. molecule H O-C-CH2 H3N. HN N H C=O common name (not the IUPAC name) NH3 ☐ H3N H ☐ CH2 Xarrow_forward> Draw the structure of alanine at pH 1.2. Click and drag to start drawing a structure.arrow_forward
- Organic And Biological ChemistryChemistryISBN:9781305081079Author:STOKER, H. Stephen (howard Stephen)Publisher:Cengage Learning,General, Organic, and Biological ChemistryChemistryISBN:9781285853918Author:H. Stephen StokerPublisher:Cengage Learning

