Concept explainers
(a)
Interpretation:
The given organic compound should be drawn as a Kekule structure or condensed structural or Bond line structure
Concept introduction:
Kekule structure: A Lewis structure in which bonded electron pairs in covalent bonds is shown as lines.
Writing organic structures in a line of text format is called condensed structural formula.
Bond line structure is a simple way of writing organic structural formula.
(b)
Interpretation:
The given organic compound should be drawn as a Kekule structure or condensed structural or Bond line structure
Concept introduction:
Kekule structure: A Lewis structure in which bonded electron pairs in covalent bonds is shown as lines.
Writing organic structures in a line of text format is called condensed structural formula.
Bond line structure is a simple way of writing organic structural formula.
(c)
Interpretation:
The given organic compound should be drawn as a Kekule structure or condensed structural or Bond line structure
Concept introduction:
Kekule structure: A Lewis structure in which bonded electron pairs in covalent bonds is shown as lines.
Writing organic structures in a line of text format is called condensed structural formula.
Bond line structure is a simple way of writing organic structural formula.
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Chemistry: Atoms First
- Draw condensed structures for three structural isomers with Chemical Formula C5H10. Name the compounds.arrow_forwardWrite the chemical formula and Lewis structure of the following, each of which contains five carbon atoms:(a) an alkane(b) an alkene(c) an alkynearrow_forward(a) Label each carbon, oxygen, and nitrogen atom as being sp, sp, or sp hybridized. (b) Circle and identify each functional group by its formal name. (c) Redraw the following compound to be a complete Lewis structure, showing all carbons, hydrogens, bonds, and nonbonded electrons. yo 이니 NECarrow_forward
- Which of the following can exist as cis/trans isomers. For any that can write both the cis and the trans structures. (a) CH2=CHCH2CH3 (b) CH3CH2CH=CHClarrow_forwardA saturated straight-chain alcohol has a molecular formula of C₆H₁₃OH. Draw the corresponding skeletal structure. C-H bonds are implied.arrow_forward2) a) b) Write the condensed structure for the following molecules: O OHarrow_forward
- 1. The structure of compound A is shown below. он NH2 (a) Redraw the above structure in the form of expanded and condensed structures. (b) Determine the number of primary, secondary, tertiary and quaternary carbon atom that can be found in the compound. (c) Redraw, circle and name the functional groups present in the compound. (d) State the possible type of stereoisomerism of the compound and draw the appropriate structures to describe the isomerism.arrow_forward(CH3)2CHOH condensed structurearrow_forwardWhat structural features help us identify a compound as(a) an alkane, (b) a cycloalkane, (c) an alkene, (d) an alkyne,(e) a saturated hydrocarbon, (f) an aromatic hydrocarbon?arrow_forward
- Draw the structural formula for each of the following compounds: (a) 2,3-dimethyloctane (b) 3-ethylheptane (c) 2,5-dimethylhexane (d) C2H4 (e) 2,2-dimethylbutanearrow_forwardA certain hydrocarbon has a molecular formula of C5H8. Which of the following is not a structural possibility for this hydrocarbon: (d) It contains an alkyne O It contains one ring and one double bond (c) It contains two double bonds and no rings O (b) It contains one ring and no double bondsarrow_forwardCan a hydrocarbon have each of the following molecular formulas? Explain why or why not in each case. (a) C 3H 8; (b) C 3H 9; (c) C 3H 6arrow_forward
- Chemistry: Principles and ReactionsChemistryISBN:9781305079373Author:William L. Masterton, Cecile N. HurleyPublisher:Cengage Learning