Concept explainers
(a)
Interpretation:
The structure of 3,3-dimethylbutane has to be drawn and correct name has to be given.
Concept Introduction:
The hydrocarbons which contains only single bonds are said to be
The Alkanes are named following some rules:
- The name of the alkane is given by the number of carbon atoms present in the chain. It is said to be Root of the alkane.
Root = number of carbon atoms in chain.
- To name the root, for one carbon atom, the root name use is meth-. For two carbon atoms, the root name is eth-, for three carbon atoms, it is prop-, for four carbon atoms, it is but-, for five carbon atoms, it is pent- and so on.
- The carbon chain is numbered in a way that the substituents get lowest number possible.
- The root name is followed by Suffix. Suffix indicates the
functional group present in the compound. It is placed after the root name.
Suffix = name of the functional group present in the compound.
- The root name also contains Prefix. Prefix is the groups attached to the root. It indicates the branched carbon atoms on the root chain and name according to the root specifying the carbon number on which it is placed. It contains –yl in name end. The prefix is placed before the root name.
Prefix = name of the branched carbon atoms on chain.
- The name of the alkane is given in the form
Prefix + Root + Suffix
(a)
Explanation of Solution
The given name of the compound is 3,3-dimethylbutane.
The structure of 3,3-dimethylbutane is given as the four carbon chain with two methyl groups as substituents at third carbon. According to the given name the structure will be given as
According to systematic nomenclature, the carbon chain should be numbered in a way that the substituents get lowest number possible. Hence, in butane four carbons are there in a chain and the methyl groups attached to the chain will get second number on the chain. So, the correct name is 2,2-dimethylbutane.
The name of the compound based on systematic nomenclature should be 2,2-dimethylbutane.
(b)
Interpretation:
The structure of 1,1,1-trimethylheptane has to be drawn and correct name has to be given.
Concept Introduction:
The hydrocarbons which contains only single bonds are said to be Alkanes. The general formula for alkanes can be given as
The Alkanes are named following some rules:
- The name of the alkane is given by the number of carbon atoms present in the chain. It is said to be Root of the alkane.
Root = number of carbon atoms in chain.
- To name the root, for one carbon atom, the root name use is meth-. For two carbon atoms, the root name is eth-, for three carbon atoms, it is prop-, for four carbon atoms, it is but-, for five carbon atoms, it is pent- and so on.
- The carbon chain is numbered in a way that the substituents get lowest number possible.
- The root name is followed by Suffix. Suffix indicates the functional group present in the compound. It is placed after the root name.
Suffix = name of the functional group present in the compound.
- The root name also contains Prefix. Prefix is the groups attached to the root. It indicates the branched carbon atoms on the root chain and name according to the root specifying the carbon number on which it is placed. It contains –yl in name end. The prefix is placed before the root name.
Prefix = name of the branched carbon atoms on chain.
- The name of the alkane is given in the form
Prefix + Root + Suffix
(b)
Explanation of Solution
The given name of the compound is 1,1,1-trimethylheptane.
The structure of 1,1,1-trimethylheptane is given as the seven carbon chain with three methyl groups as substituents at first carbon. The structure will be given as
According to systematic nomenclature, the carbon chain should be numbered in a way that the carbon chain should consists of more carbon atoms and substituents get lowest number possible.
In 1,1,1-trimethylheptane, the carbon chain consists only seven carbons with three methyl groups on first carbon. But according to the nomenclature, the carbon chain will be octane and the substituent groups are methyl groups on second carbon. The correct structure of the compound can be given as
The name of the compound based on systematic nomenclature should be 2,2-dimethyloctane.
(c)
Interpretation:
The structure of 1,4-diethylcyclopentane has to be drawn and correct name has to be given.
Concept Introduction:
The hydrocarbons which contains only single bonds are said to be Alkanes. The general formula for cycloalkanes can be given as
The cycloalkanes are named following some rules:
- The name of the cycloalkane is given by the number of carbon atoms present in the ring. It is said to be Root of the cycloalkane.
Root = number of carbon atoms in ring.
- To name the root, for one carbon atom, the root name use is meth-. For two carbon atoms, the root name is eth-, for three carbon atoms, it is prop-, for four carbon atoms, it is but-, for five carbon atoms, it is pent- and so on.
- The carbon ring is numbered in a way that the carbon with substituents get the first number in the ring.
- The root name is followed by Suffix. Suffix indicates the functional group present in the compound. It is placed after the root name.
Suffix = name of the functional group present in the compound.
- The root name also contains Prefix. Prefix is the groups attached to the root. It indicates the branched carbon atoms on the root chain and name according to the root specifying the carbon number on which it is placed. It contains –yl in name end. The prefix is placed before the root name.
Prefix = name of the branched carbon atoms on chain.
- The name of the alkane is given in the form
Prefix + Root + Suffix
(c)
Explanation of Solution
The given name of the compound is 1,4-diethylcyclopentane.
The structure of 1,4-diethylcyclopentane is given as the five carbon ring with two ethyl groups as substituents at first and fourth carbon atoms. The structure will be given as
According to systematic nomenclature, the carbon ring should be numbered in a way that the substituent containing carbon is considered as first carbon and the second substituent should get the lowest number possible in the ring.
In 1,4-diethylcyclopentane, one ethyl group is on first carbon and other ethyl group is on fourth carbon. But according to the nomenclature the substituent containing carbon is considered as first carbon and the second substituent should get the lowest number possible in the ring. The correct structure of the compound can be given as
The name of the compound based on systematic nomenclature should be 1,3-diethylcyclopentane.
(d)
Interpretation:
The structure of 1-propylcyclohexane has to be drawn and correct name has to be given.
Concept Introduction:
The hydrocarbons which contains only single bonds are said to be Alkanes. The general formula for cycloalkanes can be given as
The cycloalkanes are named following some rules:
- The name of the cycloalkane is given by the number of carbon atoms present in the ring. It is said to be Root of the cycloalkane.
Root = number of carbon atoms in ring.
- To name the root, for one carbon atom, the root name use is meth-. For two carbon atoms, the root name is eth-, for three carbon atoms, it is prop-, for four carbon atoms, it is but-, for five carbon atoms, it is pent- and so on.
- The carbon ring is numbered in a way that the carbon with substituents get the first number in the ring.
- The root name is followed by Suffix. Suffix indicates the functional group present in the compound. It is placed after the root name.
Suffix = name of the functional group present in the compound.
- The root name also contains Prefix. Prefix is the groups attached to the root. It indicates the branched carbon atoms on the root chain and name according to the root specifying the carbon number on which it is placed. It contains –yl in name end. The prefix is placed before the root name.
Prefix = name of the branched carbon atoms on chain.
- The name of the alkane is given in the form
Prefix + Root + Suffix
(d)
Explanation of Solution
The given name of the compound is 1-propylcyclohexane.
The structure of 1-propylcyclohexane is given as the six carbon ring with a propyl group as substituent at first carbon atom. The structure will be given as
According to systematic nomenclature, the carbon ring should be numbered in a way that the substituent containing carbon is considered as first carbon.
The name of the compound based on systematic nomenclature should be 1-propylcyclohexane. But it is not necessary to mention the number of the substituent on the ring (if only one substituent is present) as it will get the first position. Hence, the name of the compound will be propylcyclohexane.
Want to see more full solutions like this?
Chapter 15 Solutions
CHEMISTRY >CUSTOM<
- 4. Propose a synthesis of the target molecules from the respective starting materials. a) b) LUCH C Br OHarrow_forwardThe following mechanism for the gas phase reaction of H2 and ICI that is consistent with the observed rate law is: step 1 step 2 slow: H2(g) +ICI(g) → HCl(g) + HI(g) fast: ICI(g) + HI(g) → HCl(g) + |2(g) (1) What is the equation for the overall reaction? Use the smallest integer coefficients possible. If a box is not needed, leave it blank. + → + (2) Which species acts as a catalyst? Enter formula. If none, leave box blank: (3) Which species acts as a reaction intermediate? Enter formula. If none, leave box blank: (4) Complete the rate law for the overall reaction that is consistent with this mechanism. (Use the form k[A][B]"..., where '1' is understood (so don't write it) for m, n etc.) Rate =arrow_forwardPlease correct answer and don't use hand rating and don't use Ai solutionarrow_forward
- 1. For each of the following statements, indicate whether they are true of false. ⚫ the terms primary, secondary and tertiary have different meanings when applied to amines than they do when applied to alcohols. • a tertiary amine is one that is bonded to a tertiary carbon atom (one with three C atoms bonded to it). • simple five-membered heteroaromatic compounds (e.g. pyrrole) are typically more electron rich than benzene. ⚫ simple six-membered heteroaromatic compounds (e.g. pyridine) are typically more electron rich than benzene. • pyrrole is very weakly basic because protonation anywhere on the ring disrupts the aromaticity. • thiophene is more reactive than benzene toward electrophilic aromatic substitution. • pyridine is more reactive than nitrobenzene toward electrophilic aromatic substitution. • the lone pair on the nitrogen atom of pyridine is part of the pi system.arrow_forwardThe following reactions are NOT ordered in the way in which they occur. Reaction 1 PhO-OPh Reaction 2 Ph-O -CH₂ heat 2 *OPh Pho -CH2 Reaction 3 Ph-O ⚫OPh + -CH₂ Reaction 4 Pho Pho + H₂C OPh + CHOPh H₂C -CH₂ Reactions 1 and 3 Reaction 2 O Reaction 3 ○ Reactions 3 and 4 ○ Reactions 1 and 2 Reaction 4 ○ Reaction 1arrow_forwardSelect all possible products from the following reaction: NaOH H₂O a) b) ОН HO O HO HO e) ОН f) O HO g) h) + OHarrow_forward
- 3. Draw diagrams to represent the conjugation in these molecules. Draw two types of diagram: a. Show curly arrows linking at least two different ways of representing the molecule b. Indicate with dotted lines and partial charges (where necessary) the partial double bond (and charge) distribution H₂N* H₂N -NH2arrow_forwardQuestion 2 of 25 point Question Attempt 3 of Ulimited Draw the structure for 3-chloro-4-ethylheptane. Part 2 of 3 Click and drag to start drawing a structure. Draw the structure for 1-chloro-4-ethyl-3-lodooctane. Click and drag to start drawing a structure. X G X B c Part 3 of 30 Draw the structure for (R)-2-chlorobutane. Include the stereochemistry at all stereogenic centers. Check Click and drag to start drawing a structure. G X A 。 MacBook Pro G P Save For Later Submit Assignment Privacyarrow_forwardPlease correct answer and don't used hand raitingarrow_forward
- In a silicon and aluminum alloy, with 12.6% silicon, what are the approximate percentages of the phases present in the constituent that is formed at the end of solidification? Temperature (°C) 1500 1000 L B+L 1415- α+L 577' 500 1.65 12.6 99.83 α+B B 0 Al 20 40 60 Weight percent silicon 80 Siarrow_forwardPlease correct answer and don't used hand raitingarrow_forwardPlease correct answer and don't used hand raitingarrow_forward
- ChemistryChemistryISBN:9781305957404Author:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCostePublisher:Cengage LearningChemistryChemistryISBN:9781259911156Author:Raymond Chang Dr., Jason Overby ProfessorPublisher:McGraw-Hill EducationPrinciples of Instrumental AnalysisChemistryISBN:9781305577213Author:Douglas A. Skoog, F. James Holler, Stanley R. CrouchPublisher:Cengage Learning
- Organic ChemistryChemistryISBN:9780078021558Author:Janice Gorzynski Smith Dr.Publisher:McGraw-Hill EducationChemistry: Principles and ReactionsChemistryISBN:9781305079373Author:William L. Masterton, Cecile N. HurleyPublisher:Cengage LearningElementary Principles of Chemical Processes, Bind...ChemistryISBN:9781118431221Author:Richard M. Felder, Ronald W. Rousseau, Lisa G. BullardPublisher:WILEY