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Concept explainers
(a)
Interpretation:
The structure of the given compound is to be drawn.
Concept introduction:
The systematic naming of organic compound is given by IUPAC. The naming of organic compound is done in such a way that the structure of organic compound is correctly interpreted from the name.
Rules for writing the structural formula from IUPAC are:
• First identify the word root for the given compound.
• The suffix used in the compound like -ane, ene, yne, ol, al and so on.
• Identify the position, location, and number of the substituent bonded to the carbon chain.
(b)
Interpretation:
The structure of the given compound is to be drawn.
Concept introduction:
The systematic naming of organic compound is given by IUPAC. The naming of organic compound is done in such a way that the structure of organic compound is correctly interpreted from the name.
Rules for writing the structural formula from IUPAC are:
• First identify the word root for the given compound.
• The suffix used in the compound like –ane, ene, yne, ol, al and so on.
Identify the position, location, and number of the substituent bonded to the carbon chain.
(c)
Interpretation:
The structure of the given compound is to be drawn.
Concept introduction:
The systematic naming of organic compound is given by IUPAC. The naming of organic compound is done in such a way that the structure of organic compound is correctly interpreted from the name.
Rules for writing the structural formula from IUPAC are:
• First identify the word root for the given compound.
• The suffix used in the compound like –ane, ene, yne, ol, al and so on.
Identify the position, location, and number of the substituent bonded to the carbon chain.
(d)
Interpretation:
The structure of the given compound is to be drawn.
Concept introduction:
The systematic naming of organic compound is given by IUPAC. The naming of organic compound is done in such a way that the structure of organic compound is correctly interpreted from the name.
Rules for writing the structural formula from IUPAC are:
• First identify the word root for the given compound.
• The suffix used in the compound like –ane, ene, yne, ol, al and so on.
Identify the position, location, and number of the substituent bonded to the carbon chain.
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Chapter 8 Solutions
EBK 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-olarrow_forwardDraw the structures for the following compounds.(a) 3-benzyl-4-bromohexane , 4,4-dimethylcyclohexene(b) trans-4,5-dibromohex-2-ene , cis-1,1-dibromo-2-ethyl-2,3-dimethylcyclobutanearrow_forwardDraw the structures of the following compounds. (a) 1-chloro-1 isopropylcyclopentanearrow_forward
- Draw the skeletal structures of the following molecules.(a) (4E)-2,4-dimethyl-1,4-hexadiene (b) cis-3,3-dimethyl-4-propyl-1,5-octadiene (c) trans-2,2,5,5-tetramethyl-3-hexenearrow_forward1. (a) Draw structures of the seven isomeric alkynes of formula C6H10 - (b) Give the IUPAC and derived name of each. (c) Indicate which ones will react with Ag' or Cu(NH3)2.arrow_forwardDraw complete structural diagrams of the following compounds. (a) 2-methyl,pent-2-ene (b) propyne (c) 2,3-dimethyl butane (d) cycloheptanearrow_forward
- Give the structural formulae and name the functional groups of the following compounds. (a) 3-chlorobut-1-ene Name the functional group: (b) butanedioic acid Name the functional group: (c) propanamide Name the functional group: (d) 3-methylbutanal Name the functional group:arrow_forwardIndicate whether each statement is true or false. (a) Pentanehas a higher molar mass than hexane. (b) The longer the linearalkyl chain for straight-chain hydrocarbons, the higherthe boiling point. (c) The local geometry around the alkynegroup is linear. (d) Propane has two structural isomers.arrow_forwardGive chemical tests to distinguish between the following pairs of compounds :(a) Benzyl chloride and Chlorobenzene(b) Chloroform and Carbon tetrachloridearrow_forward
- Write structural formulas for compounds that meet the following descriptions:(a) An alkene, C6H12, that cannot have cis–trans isomersand whose longest chain is 5 carbons long(b) An alkene with a chemical formula of C10H12 that hascis–trans isomers and contains a benzene ring.arrow_forwardDraw the line formulas for the two molecules. (a) 3-ethyl-5,5-dimethyl-4-propyloctane (b) (trans)-1-bromo-2-(1,1-dimethylethyl) cyclobutanearrow_forward(1) Write a complete chemical equation showing reactants, products, and catalysts needed (if any) for the following reaction and (2) Draw and name the organic compound found in every reaction. (a) Complete hydrogenation of 2-Methylhexa-1,5-diene (b) Complete halogenation (Br2) of 3-Ethyl-2,2-dimethylhept-3-ene (c) Reaction of (4E)-2.4-Dimethylhexa-1,4-diene with a mole of water (d) Reaction of cis-3,3-Dimethyl-4-propylocta-1,5-diene with two mole of HBr (e) Reaction of trans-1-Bromo-3-chlorocyclopentane with potassium hydroxide (f) Formation of Gilman reagent using isopropyl bromide (g) Ozonolysis of 3,3-Dimethyloct-4-yne (h) Complete halogenation (Cl2) of 3-Ethyl-5-methyl-1,6,8-decatriyne (i) Partial hydrogenation using Lindlar's Catalyst 2,2,5,5-Tetramethylhex-3-yne (i) Reaction of 3.4-Dimethylcyclodecyne with sodium amidearrow_forward
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