ORGANIC CHEMISTRY, WITH SOL. MAN/ STUDY
ORGANIC CHEMISTRY, WITH SOL. MAN/ STUDY
3rd Edition
ISBN: 9781119477617
Author: Klein
Publisher: WILEY
Question
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Chapter 5, Problem 54PP

(a)

Interpretation Introduction

Interpretation:

The specific rotation of (R)-Carvone, ee, and percentage of (S)-Carvone has to be identified.

Concept Introduction:

The specific rotation (α) is a property of a chiral chemical compound. It is defined as the change in orientation of monochromatic plane-polarize light, per unit distance concentration product, as the light passes through a sample of a concentration in solution.

The specific rotation of a molecule can be calculated by using the formula given below.

[α]Tλ=αobs(degree)l(dm).C(gmL)

alpha (α) represents the observed rotation measured with a polarimeter. l represents the length of the sample tube.     C is the concentration of a solution of a pure sample.λ is the wave length of the light.

 (b)

Interpretation Introduction

Interpretation:

The specific rotation of (R)-Carvone, ee, and percentage of (S)-Carvone has to be identified.

Concept Introduction:

The specific rotation (α) is a property of a chiral chemical compound. It is defined as the change in orientation of monochromatic plane-polarize light, per unit distance concentration product, as the light passes through a sample of a concentration in solution.

The specific rotation of a molecule can be calculated by using the formula given below.

[α]Tλ=αobs(degree)l(dm).C(gmL)

alpha (α) represents the observed rotation measured with a polarimeter. l represents the length of the sample tube.     C is the concentration of a solution of a pure sample.λ is the wave length of the light.

(c)

Interpretation Introduction

Interpretation:

The specific rotation of (R)-Carvone, ee, and percentage of (S)-Carvone has to be identified.

Concept Introduction:

The specific rotation (α) is a property of a chiral chemical compound. It is defined as the change in orientation of monochromatic plane-polarize light, per unit distance concentration product, as the light passes through a sample of a concentration in solution.

The specific rotation of a molecule can be calculated by using the formula given below.

[α]Tλ=αobs(degree)l(dm).C(gmL)

alpha (α) represents the observed rotation measured with a polarimeter. l represents the length of the sample tube.     C is the concentration of a solution of a pure sample.λ is the wave length of the light.

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3. Propose a synthesis for the following transformation. Do not draw an arrow-pushing mechanism below, but make sure to draw the product of each proposed step (3 points). CN + En CN
3) Propagation of uncertainty. Every measurement has uncertainty. In this problem, we'll evaluate the uncertainty in every step of a titration of potassium hydrogen phthalate (a common acid used in titrations, abbreviated KHP, formula CsH5KO4) with NaOH of an unknown concentration. The calculation that ultimately needs to be carried out is: concentration NaOH 1000 x mass KHP × purity KHP molar mass KHP x volume NaOH Measurements: a) You use a balance to weigh 0.3992 g of KHP. The uncertainty is ±0.15 mg (0.00015 g). b) You use a buret to slowly add NaOH to the KHP until it reaches the endpoint. It takes 18.73 mL of NaOH. The uncertainty of the burst is 0.03 mL.. c) The manufacturer states the purity of KHP is 100%±0.05%. d) Even though we don't think much about them, molar masses have uncertainty as well. The uncertainty comes from the distribution of isotopes, rather than random measurement error. The uncertainty in the elements composing KHP are: a. Carbon: b. Hydrogen: ±0.0008…
Don't used hand raiting and don't used Ai solution

Chapter 5 Solutions

ORGANIC CHEMISTRY, WITH SOL. MAN/ STUDY

Ch. 5.3 - Prob. 3LTSCh. 5.3 - Prob. 9PTSCh. 5.3 - Prob. 10ATSCh. 5.4 - Prob. 4LTSCh. 5.4 - Prob. 11PTSCh. 5.4 - Prob. 12PTSCh. 5.4 - Prob. 13PTSCh. 5.4 - Prob. 14ATSCh. 5.4 - Prob. 5LTSCh. 5.4 - Prob. 15PTSCh. 5.4 - Prob. 16PTSCh. 5.4 - Prob. 17PTSCh. 5.4 - Prob. 18ATSCh. 5.5 - Prob. 6LTSCh. 5.5 - Prob. 19PTSCh. 5.5 - Prob. 20ATSCh. 5.6 - Prob. 21CCCh. 5.6 - Prob. 22CCCh. 5.6 - Prob. 23CCCh. 5.6 - Prob. 7LTSCh. 5.6 - Prob. 24PTSCh. 5.6 - Prob. 25ATSCh. 5.7 - Prob. 8LTSCh. 5.7 - Prob. 26PTSCh. 5.7 - Protease inhibitors are a class of anti-viral...Ch. 5.9 - Prob. 28CCCh. 5.11 - Prob. 9LTSCh. 5.11 - Prob. 29PTSCh. 5.11 - Prob. 30ATSCh. 5 - Prob. 31PPCh. 5 - Prob. 32PPCh. 5 - Prob. 33PPCh. 5 - Prob. 34PPCh. 5 - Prob. 35PPCh. 5 - Prob. 36PPCh. 5 - Prob. 37PPCh. 5 - Prob. 38PPCh. 5 - Prob. 39PPCh. 5 - Prob. 40PPCh. 5 - Prob. 41PPCh. 5 - Prob. 42PPCh. 5 - Prob. 43PPCh. 5 - Prob. 44PPCh. 5 - Prob. 45PPCh. 5 - Prob. 46PPCh. 5 - Prob. 47PPCh. 5 - Prob. 48PPCh. 5 - Prob. 49PPCh. 5 - Prob. 50PPCh. 5 - Prob. 51PPCh. 5 - Prob. 52PPCh. 5 - For each of the following pairs of compounds,...Ch. 5 - Prob. 54PPCh. 5 - Prob. 55PPCh. 5 - Prob. 56PPCh. 5 - Prob. 57IPCh. 5 - Prob. 58IPCh. 5 - Prob. 59IPCh. 5 - Prob. 60IPCh. 5 - There are only two stereoisomers of...Ch. 5 - Prob. 62IPCh. 5 - Prob. 63IPCh. 5 - Prob. 64IPCh. 5 - Prob. 65IPCh. 5 - Prob. 66IPCh. 5 - Prob. 67IPCh. 5 - Prob. 68IPCh. 5 - Prob. 69IPCh. 5 - Prob. 70IPCh. 5 - Prob. 71IPCh. 5 - Prob. 72IPCh. 5 - Prob. 73IPCh. 5 - Prob. 74IPCh. 5 - Prob. 75IPCh. 5 - Prob. 76IPCh. 5 - Prob. 77CPCh. 5 - Prob. 78CPCh. 5 - Prob. 79CPCh. 5 - Prob. 80CP
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