Chapter 4.13, Problem 39P

(a)

Interpretation Introduction

Interpretation:

The stereoisomers of the given compound has to be drawn.

Concept introduction:

Stereoisomers are isomers which have different spatial arrangement in spite of same bond connectivity.  Stereoisomers are due to the presence of stereocenter.  Stereocenter may be an atom axis (bond) or plane from which interchanging of two groups leads to stereoisomers.

Asymmetric center is a stereocenter which arises to hydrocarbons if the carbon is bonded to four different groups.

The equation for finding Stereoisomers from number of asymmetric centers in compounds is $2^n$, in which ‘n’ is the number of asymmetric centers.

Mesocompounds has asymmetric centers and a plane of symmetry.

(b)

Interpretation Introduction

Interpretation:

The stereoisomers of the given compound has to be drawn.

Concept introduction:

Stereoisomers are isomers which have different spatial arrangement in spite of same bond connectivity.  Stereoisomers are due to the presence of stereocenter.  Stereocenter may be an atom axis (bond) or plane from which interchanging of two groups leads to stereoisomers.

Asymmetric center is a stereocenter which arises to hydrocarbons if the carbon is bonded to four different groups.

The equation for finding Stereoisomers from number of asymmetric centers in compounds is $2^n$, in which ‘n’ is the number of asymmetric centers.

Mesocompounds has asymmetric centers and a plane of symmetry.

(c)

Interpretation Introduction

Interpretation:

The stereoisomers of the given compound has to be drawn.

Concept introduction:

Stereoisomers are isomers which have different spatial arrangement in spite of same bond connectivity. Stereoisomers are due to the presence of stereocenter.  Stereocenter may be an atom axis (bond) or plane from which interchanging of two groups leads to stereoisomers.

Asymmetric center is a stereocenter which arises to hydrocarbons if the carbon is bonded to four different groups.

The equation for finding Stereoisomers from number of asymmetric centers in compounds is $2^n$, in which ‘n’ is the number of asymmetric centers.

(d)

Interpretation Introduction

Interpretation:

The stereoisomers of the given compound has to be drawn.

Concept introduction:

Stereoisomers are isomers which have different spatial arrangement in spite of same bond connectivity. Stereoisomers are due to the presence of stereocenter.  Stereocenter may be an atom axis (bond) or plane from which interchanging of two groups leads to stereoisomers.

Asymmetric center is a stereocenter which arises to hydrocarbons if the carbon is bonded to four different groups.

The equation for finding Stereoisomers from number of asymmetric centers in compounds is $2^n$, in which ‘n’ is the number of asymmetric centers.

(e)

Interpretation Introduction

Interpretation:

The stereoisomers of the given compound has to be drawn.

Concept introduction:

Stereoisomers are isomers which have different spatial arrangement in spite of same bond connectivity.  Stereoisomers are due to the presence of stereocenter.  Stereocenter may be an atom axis (bond) or plane from which interchanging of two groups leads to stereoisomers.

Asymmetric center is a stereocenter which arises to hydrocarbons if the carbon is bonded to four different groups.

The equation for finding Stereoisomers from number of asymmetric centers in compounds is $2^n$, in which ‘n’ is the number of asymmetric centers.

Mesocompounds has asymmetric centers and a plane of symmetry.

(f)

Interpretation Introduction

Interpretation:

The stereoisomers of the given compound has to be drawn.

Concept introduction:

Stereoisomers are isomers which have different spatial arrangement in spite of same bond connectivity.  Stereoisomers are due to the presence of stereocenter.

Stereoisomers are isomers which have different spatial arrangement in spite of same bond connectivity.  Stereoisomers are due to the presence of stereocenter.  Stereocenter may be an atom axis (bond) or plane from which interchanging of two groups leads to stereoisomers.

Asymmetric center is a stereocenter which arises to hydrocarbons if the carbon is bonded to four different groups.

The equation for finding Stereoisomers from number of asymmetric centers in compounds is $2^n$, in which ‘n’ is the number of asymmetric centers.

(g)

Interpretation Introduction

Interpretation:

The stereoisomers of the given compound has to be drawn.

Concept introduction:

Stereoisomers are isomers which have different spatial arrangement in spite of same bond connectivity.  Stereoisomers are due to the presence of stereocenter.  Stereocenter may be an atom axis (bond) or plane from which interchanging of two groups leads to stereoisomers.

Asymmetric center is a stereocenter which arises to hydrocarbons if the carbon is bonded to four different groups.

The equation for finding Stereoisomers from number of asymmetric centers in compounds is $2^n$, in which ‘n’ is the number of asymmetric centers.

(h)

Interpretation Introduction

Interpretation:

The stereoisomers of the given compound has to be drawn.

Concept introduction:

Stereoisomers are isomers which have different spatial arrangement in spite of same bond connectivity.  Stereoisomers are due to the presence of stereocenter.

Stereoisomers are isomers which have different spatial arrangement in spite of same bond connectivity.  Stereoisomers are due to the presence of stereocenter.  Stereocenter may be an atom axis (bond) or plane from which interchanging of two groups leads to stereoisomers.

Asymmetric center is a stereocenter which arises to hydrocarbons if the carbon is bonded to four different groups.

The equation for finding Stereoisomers from number of asymmetric centers in compounds is $2^n$, in which ‘n’ is the number of asymmetric centers.

(i)

Interpretation Introduction

Interpretation:

The stereoisomers of the given compound has to be drawn.

Concept introduction:

Stereoisomers are isomers which have different spatial arrangement in spite of same bond connectivity.  Stereoisomers are due to the presence of stereocenter.

Stereoisomers are isomers which have different spatial arrangement in spite of same bond connectivity.  Stereoisomers are due to the presence of stereocenter.  Stereocenter may be an atom axis (bond) or plane from which interchanging of two groups leads to stereoisomers.

Asymmetric center is a stereocenter which arises to hydrocarbons if the carbon is bonded to four different groups.

The equation for finding Stereoisomers from number of asymmetric centers in compounds is $2^n$, in which ‘n’ is the number of asymmetric centers.

(j)

Interpretation Introduction

Interpretation:

The stereoisomers of the given compound has to be drawn.

Concept introduction:

Stereoisomers are isomers which have different spatial arrangement in spite of same bond connectivity.  Stereoisomers are due to the presence of stereocenter.  Stereocenter may be an atom axis (bond) or plane from which interchanging of two groups leads to stereoisomers.

Asymmetric center is a stereocenter which arises to hydrocarbons if the carbon is bonded to four different groups.

The equation for finding Stereoisomers from number of asymmetric centers in compounds is $2^n$, in which ‘n’ is the number of asymmetric centers.

(k)

Interpretation Introduction

Interpretation:

The stereoisomers of the given compound has to be drawn.

Concept introduction:

Stereoisomers are isomers which have different spatial arrangement in spite of same bond connectivity.  Stereoisomers are due to the presence of stereocenter.  Stereocenter may be an atom axis (bond) or plane from which interchanging of two groups leads to stereoisomers.

Asymmetric center is a stereocenter which arises to hydrocarbons if the carbon is bonded to four different groups.

The equation for finding Stereoisomers from number of asymmetric centers in compounds is $2^n$, in which ‘n’ is the number of asymmetric centers.

(l)

Interpretation Introduction

Interpretation:

The stereoisomers of the given compound has to be drawn.

Concept introduction:

Stereoisomers are isomers which have different spatial arrangement in spite of same bond connectivity.  Stereoisomers are due to the presence of stereocenter.  Stereocenter may be an atom axis (bond) or plane from which interchanging of two groups leads to stereoisomers.

Asymmetric center is a stereocenter which arises to hydrocarbons if the carbon is bonded to four different groups.

The equation for finding Stereoisomers from number of asymmetric centers in compounds is $2^n$, in which ‘n’ is the number of asymmetric centers.

(m)

Interpretation Introduction

Interpretation:

The stereoisomers of the given compound has to be drawn.

Concept introduction:

Stereoisomers are isomers which have different spatial arrangement in spite of same bond connectivity.  Stereoisomers are due to the presence of stereocenter.  Stereocenter may be an atom axis (bond) or plane from which interchanging of two groups leads to stereoisomers.

Asymmetric center is a stereocenter which arises to hydrocarbons if the carbon is bonded to four different groups.

The equation for finding Stereoisomers from number of asymmetric centers in compounds is $2^n$, in which ‘n’ is the number of asymmetric centers.

(n)

Interpretation Introduction

Interpretation:

The stereoisomers of the given compound has to be drawn.

Concept introduction:

Stereoisomers are isomers which have different spatial arrangement in spite of same bond connectivity.  Stereoisomers are due to the presence of stereocenter.  Stereocenter may be an atom axis (bond) or plane from which interchanging of two groups leads to stereoisomers.

Asymmetric center is a stereocenter which arises to hydrocarbons if the carbon is bonded to four different groups.

The equation for finding Stereoisomers from number of asymmetric centers in compounds is $2^n$, in which ‘n’ is the number of asymmetric centers.