
Concept explainers
(a)
Interpretation:
The structure of 4-methylhexane 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 4-methylhexane.
The structure of 4-methylhexane is given as the six carbon chain with a methyl group as substituent at fourth carbon. 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 hexane six carbons are there in a chain and the methyl group attached to the chain will get third number on the chain. So, the correct name is 3-methylhexane.
The name of the compound based on systematic nomenclature should be 3-methylhexane.
(b)
Interpretation:
The structure of 2-ethylpentane 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 2-ethylpentane.
The structure of 2-ethylpentane is given as the five carbon chain with an ethyl group as substituent at second 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 2-ethylpentane, the carbon chain consists only five carbons with an ethyl group on second carbon. But according to the nomenclature, the carbon chain will be hexane and the substituent group is methyl on third carbon. The correct structure of the compound can be given as
The name of the compound based on systematic nomenclature should be 3-methylhexane.
(c)
Interpretation:
The structure of 2-methylcyclohexane 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 2-methylcyclohexane.
The structure of 2-methylcyclohexane is given as the six carbon ring with a methyl group as substituent at second carbon. 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.
In 2-methylcyclohexane, methyl group on second carbon. But according to the nomenclature, the carbon with methyl group as substituent will be first carbon 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-methylcyclohexane. 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. The name of the compound can be given as methylcyclohexane.
(d)
Interpretation:
The structure of 3,3-methyl-4-ethyloctane 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
(d)

Explanation of Solution
The given name of the compound is 3,3-methyl-4-ethyloctane.
The structure of 3,3-methyl-4-ethyloctane is given as the eight carbon chain with two methyl groups as substituents at third carbon and an ethyl group as substituent at fourth 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. If two same groups are present as substituents on same carbon atom or different carbon atoms, prefix –di is used to mention the number of groups along with the carbon chain number on which they are present.
The structure of the given compound is correct but the name is wrong. The two methyl groups are present on the same carbon atom in the chain. To mention the number of methyl group’s present prefix –di- has to be added to the methyl.
The name of the compound based on systematic nomenclature should be 3,3-dimethyl-4-ethyloctane.
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Chapter 15 Solutions
Student Study Guide for Silberberg Chemistry: The Molecular Nature of Matter and Change
- Curved arrows are used to illustrate the flow of electrons. Using the provided starting and product structures, draw the curved electron-pushing arrows for the following reaction or mechanistic step(s). Be sure to account for all bond-breaking and bond-making steps. :0: :0 H. 0:0 :0: :6: S: :0: Select to Edit Arrows ::0 Select to Edit Arrows H :0: H :CI: Rotation Select to Edit Arrows H. < :0: :0: :0: S:arrow_forward3:48 PM Fri Apr 4 K Problem 4 of 10 Submit Curved arrows are used to illustrate the flow of electrons. Using the provided starting and product structures, draw the curved electron-pushing arrows for the following reaction or mechanistic step(s). Be sure to account for all bond-breaking and bond-making steps. Mg. :0: Select to Add Arrows :0: :Br: Mg :0: :0: Select to Add Arrows Mg. Br: :0: 0:0- Br -190 H 0:0 Select to Add Arrows Select to Add Arrows neutralizing workup H CH3arrow_forwardIarrow_forward
- Draw the Markovnikov product of the hydrobromination of this alkene. Note for advanced students: draw only one product, and don't worry about showing any stereochemistry. Drawing dash and wedge bonds has been disabled for this problem. + Explanation Check 1 X E 4 1 1 1 1 1 HBr Click and drag to start drawing a structure. 80 LE #3 @ 2 $4 0 I அ2 % 85 F * K M ? BH 2025 McGraw Hill LLC. All Rights Reserved. Terms of Use Privacy Center & 6 27 FG F10 8 9 R T Y U D F G H P J K L Z X C V B N M Q W A S H option command H command optiarrow_forwardBe sure to use wedge and dash bonds to show the stereochemistry of the products when it's important, for example to distinguish between two different major products. Predict the major products of the following reaction. Explanation Q F1 A Check F2 @ 2 # 3 + X 80 F3 W E S D $ 4 I O H. H₂ 2 R Pt % 05 LL ee F6 F5 T <6 G Click and drag to start drawing a structure. 27 & A 2025 McGraw Hill LLC. All Rights Reserved. Terms of Use Privacy Center Acce Y U H DII 8 9 F10 4 J K L Z X C V B N M T H option command F11 P H commandarrow_forwardCurved arrows are used to illustrate the flow of electrons. Use the reaction conditions provided and follow the arrows to draw the intermediate and product in this reaction or mechanistic step(s). Include all lone pairs and charges as appropriate. Ignore stereochemistry. Ignore inorganic byproducts. H :0: CH3 O: OH Q CH3OH2+ Draw Intermediate protonation CH3OH CH3OH nucleophilic addition H Draw Intermediate deprotonation :0: H3C CH3OH2* protonation H 0: H CH3 H.arrow_forward
- Predicting the reactants or products of hemiacetal and acetal formation uentify the missing organic reactants in the following reaction: H+ X+Y OH H+ за Note: This chemical equation only focuses on the important organic molecules in the reaction. Additional inorganic or small-molecule reactants or products (like H2O) are not shown. In the drawing area below, draw the skeletal ("line") structures of the missing organic reactants X and Y. You may draw the structures in any arrangement that you like, so long as they aren't touching. Explanation Check Click and drag to start drawing a structure. ? olo 18 Ar © 2025 McGraw Hill LLC. All Rights Reserved. Terms of Use | Privacy Center | Accessibilityarrow_forwardcan someone please answer thisarrow_forwardPlease, please help me figure out the the moles, molarity and Ksp column. Step by step details because I've came up with about three different number and have no idea what I'm doing wrong.arrow_forward
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