**6. Sucrose Overview**Sucrose is one of the most abundant sugars in the world. In 2017, approximately 185 million tonnes of sugar were produced worldwide. Sucrose is a chiral compound, and enantio-pure sucrose has a specific rotation of \([\alpha]^{{20}}_{D} = +66.5^\circ\).**Chemical Structure Diagram**- The image shows the chemical structure of sucrose, comprising two monosaccharides linked together.- The structure includes hydroxyl (OH) groups and a glycosidic bond between glucose and fructose units.- (+)-Sucrose is indicated in the diagram.---**Analysis of a Synthesized Sucrose Sample**A sample of synthesized sucrose from an organic chemistry lab was tested, revealing a specific rotation of \([\alpha]^{{20}}_{D} = +60.1^\circ\).**Tasks:**a) **Determine the enantiomeric excess (ee) of the sample.**b) **Calculate the ratio of two enantiomers.**c) **Draw the structure of the minor enantiomer in the sample.**---This section aims to educate on the properties and structural details of sucrose, with a focus on understanding chiral compounds and their analysis in a laboratory setting.

Given that: Specific rotation of the sample αsample is +60.1° Specific rotation of the pure sucrose…

6. Sucrose is one of the most abundant sugar in the world. About 185 million tonnes of sugar were produced worldwide in 2017. Sucrose is a chiral compound and enantio-pure sucrose has specific rotation [a]3° = +66.5°. CH2OH CH2OH ОН ОН ОН CH2OH ОН OH (+)-Sucrose A sample of synthesized sucrose from organic chemistry lab was tested, and the specific rotation of the sample is [a]3° = +60.1°. a) determine the enantiomeric excess (ee) of the sample. b) calculate the ratio of two enantiomers c) draw the structure of the minor enantiomer in the sample.

6. Sucrose is one of the most abundant sugar in the world. About 185 million tonnes of sugar were produced worldwide in 2017. Sucrose is a chiral compound and enantio-pure sucrose has specific rotation [a]3° = +66.5°. CH2OH CH2OH ОН ОН ОН CH2OH ОН OH (+)-Sucrose A sample of synthesized sucrose from organic chemistry lab was tested, and the specific rotation of the sample is [a]3° = +60.1°. a) determine the enantiomeric excess (ee) of the sample. b) calculate the ratio of two enantiomers c) draw the structure of the minor enantiomer in the sample.

Chemistry

10th Edition

ISBN:9781305957404

Author:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste

Publisher:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste

Chapter1: Chemical Foundations

Section: Chapter Questions

Problem 1RQ: Define and explain the differences between the following terms. a. law and theory b. theory and...

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Concept explainers

Alkanes and Cycloalkanes

Alkanes are saturated organic compounds which are made up of C and H atoms. Alkanes have the general formula of CnH2n+2. Alkane contains sp3 hybridized carbon atoms with four sigmas (σ) bonds & every hydrogen atom is connected with one of the carbon atoms. The size of the alkane could be determined by the number of carbon atoms located in it.

Question

**6. Sucrose Overview**

Sucrose is one of the most abundant sugars in the world. In 2017, approximately 185 million tonnes of sugar were produced worldwide. Sucrose is a chiral compound, and enantio-pure sucrose has a specific rotation of \([\alpha]^{{20}}_{D} = +66.5^\circ\).

**Chemical Structure Diagram**
- The image shows the chemical structure of sucrose, comprising two monosaccharides linked together.
- The structure includes hydroxyl (OH) groups and a glycosidic bond between glucose and fructose units.
- (+)-Sucrose is indicated in the diagram.

---

**Analysis of a Synthesized Sucrose Sample**

A sample of synthesized sucrose from an organic chemistry lab was tested, revealing a specific rotation of \([\alpha]^{{20}}_{D} = +60.1^\circ\).

**Tasks:**
a) **Determine the enantiomeric excess (ee) of the sample.**

b) **Calculate the ratio of two enantiomers.**

c) **Draw the structure of the minor enantiomer in the sample.**

---

This section aims to educate on the properties and structural details of sucrose, with a focus on understanding chiral compounds and their analysis in a laboratory setting.

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