Concept explainers
(a)
Interpretation:
All the chiral centers in the molecule are to be identified, and it is to be determined whether the molecule is meso.
Concept introduction:
A chiral center is a tetrahedral stereocenter. The atom at the chiral center must be

Answer to Problem 5.39P
The given molecule does not have any chiral center, and it is not a meso compound.
Explanation of Solution
The structure of the given molecule is
A chiral center must be an
The given molecule is determined as not a meso compound as it has no chiral center.
(b)
Interpretation:
All the chiral centers in the molecule are to be identified, and it is to be determined whether the molecule is meso.
Concept introduction:
A chiral center is a tetrahedral stereocenter. The atom at the chiral center must be

Answer to Problem 5.39P
The given molecule has one chiral center marked with
Explanation of Solution
The structure of the given molecule is
In this molecule, the nitrogen atom is a chiral center bonded to four different groups
As this molecule has only one chiral center, it cannot possess any symmetry, and hence, it is not a meso compound.
The chiral center in the given molecule is identified, and it is determined that the molecule is not a meso compound.
(c)
Interpretation:
All the chiral centers in the molecule are to be identified, and it is to be determined whether the molecule is meso.
Concept introduction:
A chiral center is a tetrahedral stereocenter. The atom at the chiral center must be

Answer to Problem 5.39P
The given molecule has one chiral center marked with
Explanation of Solution
The structure of the given molecule is
The molecule consists of a ring made up of five carbon atoms and one nitrogen atom. The nitrogen atom is bonded to three different groups having the pyramidal shape and a non-bonded electron pair pointing to the unoccupied tetrahedral corner. This makes the nitrogen a chiral center.
As this molecule has only one chiral center, it cannot possess any symmetry, and hence, it is not a meso compound. The chiral center is marked as
The chiral center in the given molecule is identified, and it is determined that the molecule is not a meso compound.
(d)
Interpretation:
All the chiral centers in the molecule are to be identified, and it is to be determined whether the molecule is meso.
Concept introduction:
The molecule with at least one chiral center having no plane of symmetry is called a chiral molecule. A chiral center is a tetrahedral stereocenter. The atom at the chiral center must be

Answer to Problem 5.39P
The given molecule has no chiral center, and it is not a meso compound.
Explanation of Solution
The structure of the given molecule is
A chiral center must be an
Therefore, these carbon atoms are also not chiral centers. As there are no chiral centers, the molecule is not a meso compound.
The given molecule is determined as not a meso compound as it has no chiral center.
(e)
Interpretation:
All the chiral centers in the molecule are to be identified, and it is to be determined whether the molecule is meso.
Concept introduction:
A chiral center is a tetrahedral stereocenter. The atom at the chiral center must be

Answer to Problem 5.39P
The molecule has two chiral centers marked with
It is not a meso compound.
Explanation of Solution
The structure of the given molecule is
The given molecule possesses two chiral carbons. One carbon is bonded to four different groups,
The molecule does not have symmetry plane; hence, it is not a meso compound.
The chiral centers in the given molecule are identified, and it is determined that the molecule is not a meso compound.
(f)
Interpretation:
All the chiral centers in the molecule are to be identified, and it is to be determined whether the molecule is meso.
Concept introduction:
A chiral center is a tetrahedral stereocenter. The atom at the chiral center must be

Answer to Problem 5.39P
The molecule has two chiral centers marked with
Explanation of Solution
The structure of the given molecule is
The given molecule possesses two chiral carbons bonded to four different groups,
The molecule has no plane of symmetry, and hence, it is not a meso compound.
The chiral centers in the given molecule are identified, and it is determined that the molecule is not a meso compound.
(g)
Interpretation:
All the chiral centers in the molecule are to be identified, and it is to be determined whether the molecule is meso.
Concept introduction:
The molecule with at least one chiral center having no plane of symmetry is called a chiral molecule. A chiral center is a tetrahedral stereocenter. The atom at the chiral center must be

Answer to Problem 5.39P
The molecule has two chiral centers marked with
Explanation of Solution
The structure of the given molecule is
The given molecule possesses two chiral carbons bonded to four different groups,
The molecule has no symmetry plane, and hence, it is not a meso compound.
The chiral centers in the given molecule are identified, and it is determined that the molecule is not a meso compound.
(h)
Interpretation:
All the chiral centers in the molecule are to be identified, and it is to be determined whether the molecule is meso.
Concept introduction:
The molecule with at least one chiral center having no plane of symmetry is called chiral molecule. A chiral center is a tetrahedral stereocenter. The atom at the chiral center must be

Answer to Problem 5.39P
The given molecule has one chiral center marked with
Explanation of Solution
The structure of the given molecule is
The molecule consists of a ring made up of four carbon atoms and one oxygen atom with a substituted methyl group. The carbon having the methyl substituent is a chiral center as it has four different groups bonded.
The molecule does not possess any symmetry plane; hence, it is a chiral molecule.
The chiral center in the given molecule is identified, and it is determined that the molecule is not a meso compound.
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Chapter 5 Solutions
EBK GET READY FOR ORGANIC CHEMISTRY
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- C A student proposes the transformation below in one step of an organic synthesis. There may be one or more products missing from the right-hand side, but there are no reagents missing from the left-hand side. There may also be catalysts, small inorganic reagents, and other important reaction conditions missing from the arrow. • Is the student's transformation possible? If not, check the box under the drawing area. . If the student's transformation is possible, then complete the reaction by adding any missing products to the right-hand side, and adding required catalysts, inorganic reagents, or other important reaction conditions above and below the arrow. • You do not need to balance the reaction, but be sure every important organic reactant or product is shown. (X) This transformation can't be done in one step. + Tarrow_forwardく Predict the major products of this organic reaction. If there aren't any products, because nothing will happen, check the box under the drawing area instead. No reaction. Explanation Check OH + + ✓ 2 H₂SO 4 O xs H₂O 2 Click and drag to start drawing a structure. © 2025 McGraw Hill LLC. All Rights Reserved. Terms of Use | Privacy Centerarrow_forwardDraw the skeletal ("line") structure of 1,3-dihydroxy-2-pentanone. Click and drag to start drawing a structure. X Parrow_forward
- Predicting edict the major products of this organic reaction. If there aren't any products, because nothing will happen, check the box under the drawing area instead. + No reaction. Explanation Check HO Na O H xs H₂O 2 Click and drag to start drawing a structure. © 2025 McGraw Hill LLC. All Rights Reserved. Terms of Use | Privacy Center Iarrow_forwardChoosing reagents and conditions for acetal formation or hydrolysis 0/5 A student proposes the transformation below in one step of an organic synthesis. There may be one or more products missing from the right-hand side, but there are no reagents missing from the left-hand side. There may also be catalysts, small inorganic reagents, and other important reaction conditions missing from the arrow. • Is the student's transformation possible? If not, check the box under the drawing area. If the student's transformation is possible, then complete the reaction by adding any missing products to the right-hand side, and adding required catalysts, inorganic reagents, or other important reaction conditions above and below the arrow. • You do not need to balance the reaction, but be sure every important organic reactant or product is shown. + This transformation can't be done in one step. 5 I H Autumn alo 值 Ar Barrow_forwardA block of copper of mass 2.00kg(cp = 0.3851 .K) and g temperature 0°C is introduced into an insulated container in which there is 1.00molH, O(g) at 100°C and 1.00 2 atm. Note that C P = 4.184. K for liquid water, and g that A H = 2260 for water. vap g Assuming all the steam is condensed to water, and that the pressure remains constant: (a) What will be the final temperature of the system? (b) What is the heat transferred from the water to the copper? (c) What is the entropy change of the water, the copper, and the total system?arrow_forward
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