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There are eight different five-carbon alkyl groups.

(a) Draw them

(b) Give them systematic names.

(c) In each case, label the degree of substitution (primary, secondary, or tertiary) of the head carbon atom bonded to the main chain.

Short Answer

Expert verified

Alkanes are hydrocarbons containing only single bonds. The general formula for an alkane is CnH2n+2, where n = the number of carbon atoms.

Step by step solution

01

Alkanes

Alkanes are hydrocarbons containing only single bonds. The general formula for an alkane is CnH2n+2, where n = the number of carbon atoms.

02

Alkyl groups

The alkyl groups are named by replacing the suffix (-ane) of the alkane name with -yl.

03

Rules for naming alkanes

In order for an alkane to be named, following rules must be followed.

(a) The longest continuous chain of carbon atoms is identified, which gives the base name.

(b) Starting with the end nearest a branch, the longest carbon chain is numbered.

(c) Substituents present on the longest chain, such as alkyl groups, are named, and each substituent is located by the number of the main chain carbon atom to which it is attached.

(d) Listing can be done in alphabetical order if two or more substituents are present. Prefixes like di-, tri-, tetra-, etc., are used if there are two or more of the same alkyl substituents.

04

Drawing, naming, and labeling the degree of substitution in eight different five-carbon alkyl groups

Eight different five-carbon alkyl groups are pentyl, terc-pentyl, neopentyl, isopentyl, sec-pentyl, 3-pentyl, sec-isopentyl, and active pentyl.


Labelling the degree of substitution in eight different five-carbon alkyl groups

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Most popular questions from this chapter

Each of the following descriptions applies to more than one alkane. In each case draw and name two structures that match the description.

(a)²¹²Ô â¶Ä‰i²õ´Ç±è°ù´Ç±è²â±ô³ó±ð±è³Ù²¹²Ô±ð

(b)²¹â€‰d¾±±ð³Ù³ó²â±ô»å±ð³¦²¹²Ô±ð

(c)acis −diethylcyclohexane

(d)atrans −dihalocyclopentane

(e)a(2,3-dimethylpentyl)cycloalkane

(f)²¹â€‰â¶Ä‰b¾±³¦²â³¦±ô´Ç²Ô´Ç²Ô²¹²Ô±ð


Construct a graph, similar to Figure 3-11, of the torsional energy of 3-methylpentanealong theC2−C3.PlaceC2in front, represented by three bonds coming together in a Y shape, andC3in back, represented by a circle with three bonds pointing out from it. Define the dihedral angle as the angle between the methyl group on the front carbon and ethyl group on the back carbon. Begin your graph at 00thedihedral angle and begin to turn the front carbon. Show the Newman projection and the approximate energy at each600of rotation. Indicate which conformations are the most stable (lowest energy) and the least stable (highest energy).

Question: Convert each Newman projection to the equivalent line-angle formula, and assign the IUPAC name.

List each set of compounds in order of increasing boiling point.

(a) hexane, octane, and decane

(b) octane, (CH3)3C-C(CH3)3, and CH3CH2C(CH3)2CH2CH2CH3

Which of the following structures represent the same compounds. Whichof the following compounds represents different ones.

(a)

(b)

(c)

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