CHEMISTRY: THE MOLECULAR NATURE OF MATTE
CHEMISTRY: THE MOLECULAR NATURE OF MATTE
9th Edition
ISBN: 9781265974688
Author: SILBERBERG
Publisher: MCG
Question
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Chapter 15.2, Problem 15.2AP

(a)

Interpretation Introduction

Interpretation:

The systematic name for the below given compound has to be given.

CHEMISTRY: THE MOLECULAR NATURE OF MATTE, Chapter 15.2, Problem 15.2AP , additional homework tip  1

Concept Introduction:

The hydrocarbons which contains only single bonds are said to be Alkanes.  The general formula for alkanes can be given as CnH2n+2.  All carbon atoms are sp3 hybridized.

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 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)

Interpretation Introduction

Interpretation:

The systematic name for the below given compound has to be given.

CHEMISTRY: THE MOLECULAR NATURE OF MATTE, Chapter 15.2, Problem 15.2AP , additional homework tip  2

Concept Introduction:

The hydrocarbons which contains only single bonds are said to be Alkanes.  When alkane loses two hydrogens and forms a cyclic ring, it is said to be cycloalkane.  The general formula for cycloalkanes can be given as CnH2n.

The Alkanes 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 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 ring 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 ring.

  • The name of the cycloalkane is given in the form

Prefix + Root + Suffix

(c)

Interpretation Introduction

Interpretation:

The systematic name for the given compound has to be given and the geometric isomer present in the compound has to be identified.

CHEMISTRY: THE MOLECULAR NATURE OF MATTE, Chapter 15.2, Problem 15.2AP , additional homework tip  3

Concept Introduction:

The hydrocarbons which contains double bonds are said to be Alkenes.  When alkane loses two hydrogens and forms a double bond, it is said to be alkene.  The general formula for alkenes can be given as CnH2n.

The Alkenes are named following some rules:

  • The name of the alkene is given by the number of carbon atoms including the double bonded carbon atoms in the chain.  It is said to be Root of the alkene.

Root = number of carbon atoms in chain including the double bond.

  • 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 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 ring 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 ring.

  • The name of the cycloalkane is given in the form

Prefix + Root + Suffix

The geometrical isomers have different orientations of groups around a double bond.  The geometric isomers are cis-trans isomers.  The isomer which contains same groups or equally prioritized groups on the same side of the double bonded carbon atoms, it is said to be cis-isomer.  If the same groups or equally prioritized groups are present on the opposite sides of the double bonded carbon atoms, it is said to be trans-isomer.

(d)

Interpretation Introduction

Interpretation:

The systematic name for the given compound has to be given and the chiral centers has to be identified.

CHEMISTRY: THE MOLECULAR NATURE OF MATTE, Chapter 15.2, Problem 15.2AP , additional homework tip  4

Concept Introduction:

The hydrocarbons which contains only single bonds are said to be Alkanes.  When alkane loses two hydrogens and forms a cyclic ring, it is said to be cycloalkane.  The general formula for cycloalkanes can be given as CnH2n.

The Alkanes 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 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 ring 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 ring.

  • The name of the cycloalkane is given in the form

Prefix + Root + Suffix

The atom is said to be as chiral when it is attached to four different groups.  It is asymmetrical and does not super-impose on its mirror image.  In a compound, the atom which is asymmetric is chiral and is called chiral centre.

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Chapter 15 Solutions

CHEMISTRY: THE MOLECULAR NATURE OF MATTE

Ch. 15.4 - Prob. 15.4BFPCh. 15.4 - Prob. 15.5AFPCh. 15.4 - Prob. 15.5BFPCh. 15.4 - Prob. 15.6AFPCh. 15.4 - Prob. 15.6BFPCh. 15.4 - Prob. 15.7AFPCh. 15.4 - Prob. 15.7BFPCh. 15.6 - Prob. 15.4PCh. 15.6 - Prob. 15.5PCh. 15 - Prob. 15.1PCh. 15 - Prob. 15.2PCh. 15 - Prob. 15.3PCh. 15 - Silicon lies just below carbon in Group 4A(14) and...Ch. 15 - What is the range of oxidation states for carbon?...Ch. 15 - Prob. 15.6PCh. 15 - Prob. 15.7PCh. 15 - Define each type of isomer: (a) constitutional;...Ch. 15 - Prob. 15.9PCh. 15 - Prob. 15.10PCh. 15 - Prob. 15.11PCh. 15 - How does an aromatic hydrocarbon differ from a...Ch. 15 - Prob. 15.13PCh. 15 - Prob. 15.14PCh. 15 - Prob. 15.15PCh. 15 - Prob. 15.16PCh. 15 - Prob. 15.17PCh. 15 - Prob. 15.18PCh. 15 - Prob. 15.19PCh. 15 - Prob. 15.20PCh. 15 - Prob. 15.21PCh. 15 - Prob. 15.22PCh. 15 - Prob. 15.23PCh. 15 - Prob. 15.24PCh. 15 - Draw structures from the following names, and...Ch. 15 - Prob. 15.26PCh. 15 - Prob. 15.27PCh. 15 - Prob. 15.28PCh. 15 - Prob. 15.29PCh. 15 - Prob. 15.30PCh. 15 - Prob. 15.31PCh. 15 - Prob. 15.32PCh. 15 - Prob. 15.33PCh. 15 - Prob. 15.34PCh. 15 - Prob. 15.35PCh. 15 - Prob. 15.36PCh. 15 - Prob. 15.37PCh. 15 - Prob. 15.38PCh. 15 - Prob. 15.39PCh. 15 - Prob. 15.40PCh. 15 - Determine the type of each of the following...Ch. 15 - Prob. 15.42PCh. 15 - Prob. 15.43PCh. 15 - Prob. 15.44PCh. 15 - Prob. 15.45PCh. 15 - Prob. 15.46PCh. 15 - Prob. 15.47PCh. 15 - Prob. 15.48PCh. 15 - Prob. 15.49PCh. 15 - Prob. 15.50PCh. 15 - Prob. 15.51PCh. 15 - Prob. 15.52PCh. 15 - Prob. 15.53PCh. 15 - Prob. 15.54PCh. 15 - Prob. 15.55PCh. 15 - Prob. 15.56PCh. 15 - Prob. 15.57PCh. 15 - Prob. 15.58PCh. 15 - Prob. 15.59PCh. 15 - Prob. 15.60PCh. 15 - Prob. 15.61PCh. 15 - Prob. 15.62PCh. 15 - Prob. 15.63PCh. 15 - Prob. 15.64PCh. 15 - Prob. 15.65PCh. 15 - Prob. 15.66PCh. 15 - Prob. 15.67PCh. 15 - Prob. 15.68PCh. 15 - Prob. 15.69PCh. 15 - Prob. 15.70PCh. 15 - Prob. 15.71PCh. 15 - Prob. 15.72PCh. 15 - Prob. 15.73PCh. 15 - Prob. 15.74PCh. 15 - Prob. 15.75PCh. 15 - Prob. 15.76PCh. 15 - Prob. 15.77PCh. 15 - Prob. 15.78PCh. 15 - Prob. 15.79PCh. 15 - Prob. 15.80PCh. 15 - Prob. 15.81PCh. 15 - Prob. 15.82PCh. 15 - Prob. 15.83PCh. 15 - Prob. 15.84PCh. 15 - Prob. 15.85PCh. 15 - Prob. 15.86PCh. 15 - Prob. 15.87PCh. 15 - What is the key structural difference between...Ch. 15 - Protein shape, function, and amino acid sequence...Ch. 15 - What linkage joins the monomers in each strand of...Ch. 15 - What is base pairing? How does it pertain to DNA...Ch. 15 - RNA base sequence, protein amino acid sequence,...Ch. 15 - Prob. 15.93PCh. 15 - Prob. 15.94PCh. 15 - Draw the structure of each of the following...Ch. 15 - Prob. 15.96PCh. 15 - Write the sequence of the complementary DNA strand...Ch. 15 - Prob. 15.98PCh. 15 - Prob. 15.99PCh. 15 - Prob. 15.100PCh. 15 - Prob. 15.101PCh. 15 - Amino acids have an average molar mass of 100...Ch. 15 - Prob. 15.103PCh. 15 - Prob. 15.104PCh. 15 - Some of the most useful compounds for organic...Ch. 15 - Prob. 15.106PCh. 15 - Prob. 15.107PCh. 15 - Prob. 15.108PCh. 15 - Prob. 15.109PCh. 15 - Prob. 15.110PCh. 15 - Prob. 15.111PCh. 15 - Prob. 15.112PCh. 15 - The polypeptide chain in proteins does not exhibit...Ch. 15 - Prob. 15.114PCh. 15 - Prob. 15.115PCh. 15 - Prob. 15.116PCh. 15 - Prob. 15.117PCh. 15 - Wastewater from a cheese factory has the following...Ch. 15 - Prob. 15.119P
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