(a) Interpretation: The amino acid in Fischer projection and interpret it as D- or L- enantiomer. Concept introduction: Fischer projections are the representation of bonds by using horizontal and vertical lines in the 3D state. The horizontal lines represent the bonds that are out of paper towards the vision and the vertical lines represent the bonds pointing out the back of the paper away from vision. The intersection between the two lines represents the carbon atom. A carbon which has all the four different atoms or group of atoms has tetrahedral geometry and such carbon molecule is referred to as the chiral carbon. The two different forms in which a single chiral center can exist is referred to as enantiomers. Simply, the substances which show optical isomerism exist as two isomers known as enantiomers. Enantiomers are non-super imposable mirror images of each other. The number of enantiomers of a molecule depends on the number of chiral centers. Pictorial representation: The Fischer projection of the given amino acidvaline is represented as below: Fig. 1(a): Fischer projection of valine.

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Answer 1

Question

Chapter 5, Problem 3P

Interpretation Introduction

(a) Interpretation:

The amino acid in Fischer projection and interpret it as D- or L- enantiomer.

Concept introduction:

Fischer projections are the representation of bonds by using horizontal and vertical lines in the 3D state. The horizontal lines represent the bonds that are out of paper towards the vision and the vertical lines represent the bonds pointing out the back of the paper away from vision. The intersection between the two lines represents the carbon atom.

A carbon which has all the four different atoms or group of atoms has tetrahedral geometry and such carbon molecule is referred to as the chiral carbon. The two different forms in which a single chiral center can exist is referred to as enantiomers. Simply, the substances which show optical isomerism exist as two isomers known as enantiomers. Enantiomers are non-super imposable mirror images of each other. The number of enantiomers of a molecule depends on the number of chiral centers.

Pictorial representation:

The Fischer projection of the given amino acidvaline is represented as below:

Fig. 1(a): Fischer projection of valine.

Interpretation Introduction

(b) Interpretation:

The amino acid in Fischer projection and interpret it as D- or L- enantiomer.

Concept introduction:

Fischer projections are the representation of bonds by using horizontal and vertical lines in the 3D state. The horizontal lines represent the bonds that are out of paper towards the vision and the vertical lines represent the bonds pointing out the back of the paper away from vision. The intersection between the two lines represents the carbon atom.

A carbon which has all the four different atoms or group of atoms has tetrahedral geometry and such carbon molecule is referred to as the chiral carbon. The two different forms in which a single chiral center can exist is referred to as enantiomers. Simply, the substances which show optical isomerism exist as two isomers known as enantiomers. Enantiomers are non-super imposable mirror images of each other. The number of enantiomers of a molecule depends on the number of chiral centers.

Pictorial representation:

The Fischer projection of threonine is represented as below.

Fig. 2(a): Fischer projection of threonine.

Interpretation Introduction

(c) Interpretation:

The amino acid in Fischer projection and interpret it as D- or L- enantiomer.

Concept introduction:

Fischer projections are the representation of bonds by using horizontal and vertical lines in the 3D state. The horizontal lines represent the bonds that are out of paper towards the vision and the vertical lines represent the bonds pointing out the back of the paper away from vision. The intersection between the two lines represents the carbon atom.

A carbon which has all the four different atoms or group of atoms has tetrahedral geometry and such carbon molecule is referred to as the chiral carbon. The two different forms in which a single chiral center can exist is referred to as enantiomers. Simply, the substances which show optical isomerism exist as two isomers known as enantiomers. Enantiomers are non-super imposable mirror images of each other. The number of enantiomers of a molecule depends on the number of chiral centers.

Pictorial representation:

The Fischer projection of glutamine is represented as below:

Fig. 3(a): Fischer projection of glutamine.

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Please help determine the standard curve for my Kinase Activity in Excel Spreadsheet. Link: https://mnscu-my.sharepoint.com/personal/vi2163ss_go_minnstate_edu/_layouts/15/Doc.aspx?sourcedoc=%7B958f5aee-aabd-45d7-9f7e-380002892ee0%7D&action=default&slrid=9b178ea1-b025-8000-6e3f-1cbfb0aaef90&originalPath=aHR0cHM6Ly9tbnNjdS1teS5zaGFyZXBvaW50LmNvbS86eDovZy9wZXJzb25hbC92aTIxNjNzc19nb19taW5uc3RhdGVfZWR1L0VlNWFqNVc5cXRkRm4zNDRBQUtKTHVBQldtcEtWSUdNVmtJMkoxQzl3dmtPVlE_cnRpbWU9eEE2X291ZHIzVWc&CID=e2126631-9922-4cc5-b5d3-54c7007a756f&_SRM=0:G:93 Determine the amount of VRK1 is present 1. Average the data and calculate the mean absorbance for each concentration/dilution (Please over look for Corrections) 2. Blank Correction à Subtract 0 ug/mL blank absorbance from all readings (Please over look for Corrections) 3. Plot the Standard Curve (Please over look for Corrections) 4. Convert VRK1 concentration from ug/mL to g/L 5. Use the molar mass of VRK1 to convert to M and uM…

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Answer 2

Question

Chapter 5, Problem 3P

Interpretation Introduction

(a) Interpretation:

The amino acid in Fischer projection and interpret it as D- or L- enantiomer.

Concept introduction:

Fischer projections are the representation of bonds by using horizontal and vertical lines in the 3D state. The horizontal lines represent the bonds that are out of paper towards the vision and the vertical lines represent the bonds pointing out the back of the paper away from vision. The intersection between the two lines represents the carbon atom.

A carbon which has all the four different atoms or group of atoms has tetrahedral geometry and such carbon molecule is referred to as the chiral carbon. The two different forms in which a single chiral center can exist is referred to as enantiomers. Simply, the substances which show optical isomerism exist as two isomers known as enantiomers. Enantiomers are non-super imposable mirror images of each other. The number of enantiomers of a molecule depends on the number of chiral centers.

Pictorial representation:

The Fischer projection of the given amino acidvaline is represented as below:

Fig. 1(a): Fischer projection of valine.

Interpretation Introduction

(b) Interpretation:

The amino acid in Fischer projection and interpret it as D- or L- enantiomer.

Concept introduction:

Fischer projections are the representation of bonds by using horizontal and vertical lines in the 3D state. The horizontal lines represent the bonds that are out of paper towards the vision and the vertical lines represent the bonds pointing out the back of the paper away from vision. The intersection between the two lines represents the carbon atom.

A carbon which has all the four different atoms or group of atoms has tetrahedral geometry and such carbon molecule is referred to as the chiral carbon. The two different forms in which a single chiral center can exist is referred to as enantiomers. Simply, the substances which show optical isomerism exist as two isomers known as enantiomers. Enantiomers are non-super imposable mirror images of each other. The number of enantiomers of a molecule depends on the number of chiral centers.

Pictorial representation:

The Fischer projection of threonine is represented as below.

Fig. 2(a): Fischer projection of threonine.

Interpretation Introduction

(c) Interpretation:

The amino acid in Fischer projection and interpret it as D- or L- enantiomer.

Concept introduction:

Fischer projections are the representation of bonds by using horizontal and vertical lines in the 3D state. The horizontal lines represent the bonds that are out of paper towards the vision and the vertical lines represent the bonds pointing out the back of the paper away from vision. The intersection between the two lines represents the carbon atom.

A carbon which has all the four different atoms or group of atoms has tetrahedral geometry and such carbon molecule is referred to as the chiral carbon. The two different forms in which a single chiral center can exist is referred to as enantiomers. Simply, the substances which show optical isomerism exist as two isomers known as enantiomers. Enantiomers are non-super imposable mirror images of each other. The number of enantiomers of a molecule depends on the number of chiral centers.

Pictorial representation:

The Fischer projection of glutamine is represented as below:

Fig. 3(a): Fischer projection of glutamine.

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Answer 3

Question

Chapter 5, Problem 3P

Interpretation Introduction

(a) Interpretation:

The amino acid in Fischer projection and interpret it as D- or L- enantiomer.

Concept introduction:

Fischer projections are the representation of bonds by using horizontal and vertical lines in the 3D state. The horizontal lines represent the bonds that are out of paper towards the vision and the vertical lines represent the bonds pointing out the back of the paper away from vision. The intersection between the two lines represents the carbon atom.

A carbon which has all the four different atoms or group of atoms has tetrahedral geometry and such carbon molecule is referred to as the chiral carbon. The two different forms in which a single chiral center can exist is referred to as enantiomers. Simply, the substances which show optical isomerism exist as two isomers known as enantiomers. Enantiomers are non-super imposable mirror images of each other. The number of enantiomers of a molecule depends on the number of chiral centers.

Pictorial representation:

The Fischer projection of the given amino acidvaline is represented as below:

Fig. 1(a): Fischer projection of valine.

Interpretation Introduction

(b) Interpretation:

The amino acid in Fischer projection and interpret it as D- or L- enantiomer.

Concept introduction:

Fischer projections are the representation of bonds by using horizontal and vertical lines in the 3D state. The horizontal lines represent the bonds that are out of paper towards the vision and the vertical lines represent the bonds pointing out the back of the paper away from vision. The intersection between the two lines represents the carbon atom.

A carbon which has all the four different atoms or group of atoms has tetrahedral geometry and such carbon molecule is referred to as the chiral carbon. The two different forms in which a single chiral center can exist is referred to as enantiomers. Simply, the substances which show optical isomerism exist as two isomers known as enantiomers. Enantiomers are non-super imposable mirror images of each other. The number of enantiomers of a molecule depends on the number of chiral centers.

Pictorial representation:

The Fischer projection of threonine is represented as below.

Fig. 2(a): Fischer projection of threonine.

Interpretation Introduction

(c) Interpretation:

The amino acid in Fischer projection and interpret it as D- or L- enantiomer.

Concept introduction:

Fischer projections are the representation of bonds by using horizontal and vertical lines in the 3D state. The horizontal lines represent the bonds that are out of paper towards the vision and the vertical lines represent the bonds pointing out the back of the paper away from vision. The intersection between the two lines represents the carbon atom.

A carbon which has all the four different atoms or group of atoms has tetrahedral geometry and such carbon molecule is referred to as the chiral carbon. The two different forms in which a single chiral center can exist is referred to as enantiomers. Simply, the substances which show optical isomerism exist as two isomers known as enantiomers. Enantiomers are non-super imposable mirror images of each other. The number of enantiomers of a molecule depends on the number of chiral centers.

Pictorial representation:

The Fischer projection of glutamine is represented as below:

Fig. 3(a): Fischer projection of glutamine.

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Answer 4

Question

Chapter 5, Problem 3P

Interpretation Introduction

(a) Interpretation:

The amino acid in Fischer projection and interpret it as D- or L- enantiomer.

Concept introduction:

Fischer projections are the representation of bonds by using horizontal and vertical lines in the 3D state. The horizontal lines represent the bonds that are out of paper towards the vision and the vertical lines represent the bonds pointing out the back of the paper away from vision. The intersection between the two lines represents the carbon atom.

A carbon which has all the four different atoms or group of atoms has tetrahedral geometry and such carbon molecule is referred to as the chiral carbon. The two different forms in which a single chiral center can exist is referred to as enantiomers. Simply, the substances which show optical isomerism exist as two isomers known as enantiomers. Enantiomers are non-super imposable mirror images of each other. The number of enantiomers of a molecule depends on the number of chiral centers.

Pictorial representation:

The Fischer projection of the given amino acidvaline is represented as below:

Fig. 1(a): Fischer projection of valine.

Interpretation Introduction

(b) Interpretation:

The amino acid in Fischer projection and interpret it as D- or L- enantiomer.

Concept introduction:

Fischer projections are the representation of bonds by using horizontal and vertical lines in the 3D state. The horizontal lines represent the bonds that are out of paper towards the vision and the vertical lines represent the bonds pointing out the back of the paper away from vision. The intersection between the two lines represents the carbon atom.

A carbon which has all the four different atoms or group of atoms has tetrahedral geometry and such carbon molecule is referred to as the chiral carbon. The two different forms in which a single chiral center can exist is referred to as enantiomers. Simply, the substances which show optical isomerism exist as two isomers known as enantiomers. Enantiomers are non-super imposable mirror images of each other. The number of enantiomers of a molecule depends on the number of chiral centers.

Pictorial representation:

The Fischer projection of threonine is represented as below.

Fig. 2(a): Fischer projection of threonine.

Interpretation Introduction

(c) Interpretation:

The amino acid in Fischer projection and interpret it as D- or L- enantiomer.

Concept introduction:

Fischer projections are the representation of bonds by using horizontal and vertical lines in the 3D state. The horizontal lines represent the bonds that are out of paper towards the vision and the vertical lines represent the bonds pointing out the back of the paper away from vision. The intersection between the two lines represents the carbon atom.

A carbon which has all the four different atoms or group of atoms has tetrahedral geometry and such carbon molecule is referred to as the chiral carbon. The two different forms in which a single chiral center can exist is referred to as enantiomers. Simply, the substances which show optical isomerism exist as two isomers known as enantiomers. Enantiomers are non-super imposable mirror images of each other. The number of enantiomers of a molecule depends on the number of chiral centers.

Pictorial representation:

The Fischer projection of glutamine is represented as below:

Fig. 3(a): Fischer projection of glutamine.

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Answer 5

Chapter 5, Problem 3P

Interpretation Introduction

(a) Interpretation:

The amino acid in Fischer projection and interpret it as D- or L- enantiomer.

Concept introduction:

Fischer projections are the representation of bonds by using horizontal and vertical lines in the 3D state. The horizontal lines represent the bonds that are out of paper towards the vision and the vertical lines represent the bonds pointing out the back of the paper away from vision. The intersection between the two lines represents the carbon atom.

A carbon which has all the four different atoms or group of atoms has tetrahedral geometry and such carbon molecule is referred to as the chiral carbon. The two different forms in which a single chiral center can exist is referred to as enantiomers. Simply, the substances which show optical isomerism exist as two isomers known as enantiomers. Enantiomers are non-super imposable mirror images of each other. The number of enantiomers of a molecule depends on the number of chiral centers.

Pictorial representation:

The Fischer projection of the given amino acidvaline is represented as below:

Fig. 1(a): Fischer projection of valine.

Interpretation Introduction

(b) Interpretation:

The amino acid in Fischer projection and interpret it as D- or L- enantiomer.

Concept introduction:

Fischer projections are the representation of bonds by using horizontal and vertical lines in the 3D state. The horizontal lines represent the bonds that are out of paper towards the vision and the vertical lines represent the bonds pointing out the back of the paper away from vision. The intersection between the two lines represents the carbon atom.

A carbon which has all the four different atoms or group of atoms has tetrahedral geometry and such carbon molecule is referred to as the chiral carbon. The two different forms in which a single chiral center can exist is referred to as enantiomers. Simply, the substances which show optical isomerism exist as two isomers known as enantiomers. Enantiomers are non-super imposable mirror images of each other. The number of enantiomers of a molecule depends on the number of chiral centers.

Pictorial representation:

The Fischer projection of threonine is represented as below.

Fig. 2(a): Fischer projection of threonine.

Interpretation Introduction

(c) Interpretation:

The amino acid in Fischer projection and interpret it as D- or L- enantiomer.

Concept introduction:

Fischer projections are the representation of bonds by using horizontal and vertical lines in the 3D state. The horizontal lines represent the bonds that are out of paper towards the vision and the vertical lines represent the bonds pointing out the back of the paper away from vision. The intersection between the two lines represents the carbon atom.

A carbon which has all the four different atoms or group of atoms has tetrahedral geometry and such carbon molecule is referred to as the chiral carbon. The two different forms in which a single chiral center can exist is referred to as enantiomers. Simply, the substances which show optical isomerism exist as two isomers known as enantiomers. Enantiomers are non-super imposable mirror images of each other. The number of enantiomers of a molecule depends on the number of chiral centers.

Pictorial representation:

The Fischer projection of glutamine is represented as below:

Fig. 3(a): Fischer projection of glutamine.

Answer 6

Chapter 5, Problem 3P

Interpretation Introduction

(a) Interpretation:

The amino acid in Fischer projection and interpret it as D- or L- enantiomer.

Concept introduction:

Fischer projections are the representation of bonds by using horizontal and vertical lines in the 3D state. The horizontal lines represent the bonds that are out of paper towards the vision and the vertical lines represent the bonds pointing out the back of the paper away from vision. The intersection between the two lines represents the carbon atom.

A carbon which has all the four different atoms or group of atoms has tetrahedral geometry and such carbon molecule is referred to as the chiral carbon. The two different forms in which a single chiral center can exist is referred to as enantiomers. Simply, the substances which show optical isomerism exist as two isomers known as enantiomers. Enantiomers are non-super imposable mirror images of each other. The number of enantiomers of a molecule depends on the number of chiral centers.

Pictorial representation:

The Fischer projection of the given amino acidvaline is represented as below:

Fig. 1(a): Fischer projection of valine.

Answer 7

Chapter 5, Problem 3P

Interpretation Introduction

(a) Interpretation:

The amino acid in Fischer projection and interpret it as D- or L- enantiomer.

Concept introduction:

Fischer projections are the representation of bonds by using horizontal and vertical lines in the 3D state. The horizontal lines represent the bonds that are out of paper towards the vision and the vertical lines represent the bonds pointing out the back of the paper away from vision. The intersection between the two lines represents the carbon atom.

A carbon which has all the four different atoms or group of atoms has tetrahedral geometry and such carbon molecule is referred to as the chiral carbon. The two different forms in which a single chiral center can exist is referred to as enantiomers. Simply, the substances which show optical isomerism exist as two isomers known as enantiomers. Enantiomers are non-super imposable mirror images of each other. The number of enantiomers of a molecule depends on the number of chiral centers.

Pictorial representation:

The Fischer projection of the given amino acidvaline is represented as below:

Fig. 1(a): Fischer projection of valine.

Answer 8

Interpretation Introduction

(b) Interpretation:

The amino acid in Fischer projection and interpret it as D- or L- enantiomer.

Concept introduction:

Fischer projections are the representation of bonds by using horizontal and vertical lines in the 3D state. The horizontal lines represent the bonds that are out of paper towards the vision and the vertical lines represent the bonds pointing out the back of the paper away from vision. The intersection between the two lines represents the carbon atom.

A carbon which has all the four different atoms or group of atoms has tetrahedral geometry and such carbon molecule is referred to as the chiral carbon. The two different forms in which a single chiral center can exist is referred to as enantiomers. Simply, the substances which show optical isomerism exist as two isomers known as enantiomers. Enantiomers are non-super imposable mirror images of each other. The number of enantiomers of a molecule depends on the number of chiral centers.

Pictorial representation:

The Fischer projection of threonine is represented as below.

Fig. 2(a): Fischer projection of threonine.

Answer 9

Interpretation Introduction

(b) Interpretation:

The amino acid in Fischer projection and interpret it as D- or L- enantiomer.

Concept introduction:

Fischer projections are the representation of bonds by using horizontal and vertical lines in the 3D state. The horizontal lines represent the bonds that are out of paper towards the vision and the vertical lines represent the bonds pointing out the back of the paper away from vision. The intersection between the two lines represents the carbon atom.

A carbon which has all the four different atoms or group of atoms has tetrahedral geometry and such carbon molecule is referred to as the chiral carbon. The two different forms in which a single chiral center can exist is referred to as enantiomers. Simply, the substances which show optical isomerism exist as two isomers known as enantiomers. Enantiomers are non-super imposable mirror images of each other. The number of enantiomers of a molecule depends on the number of chiral centers.

Pictorial representation:

The Fischer projection of threonine is represented as below.

Fig. 2(a): Fischer projection of threonine.

Answer 10

Interpretation Introduction

(c) Interpretation:

The amino acid in Fischer projection and interpret it as D- or L- enantiomer.

Concept introduction:

Fischer projections are the representation of bonds by using horizontal and vertical lines in the 3D state. The horizontal lines represent the bonds that are out of paper towards the vision and the vertical lines represent the bonds pointing out the back of the paper away from vision. The intersection between the two lines represents the carbon atom.

A carbon which has all the four different atoms or group of atoms has tetrahedral geometry and such carbon molecule is referred to as the chiral carbon. The two different forms in which a single chiral center can exist is referred to as enantiomers. Simply, the substances which show optical isomerism exist as two isomers known as enantiomers. Enantiomers are non-super imposable mirror images of each other. The number of enantiomers of a molecule depends on the number of chiral centers.

Pictorial representation:

The Fischer projection of glutamine is represented as below:

Fig. 3(a): Fischer projection of glutamine.

Answer 11

Interpretation Introduction

(c) Interpretation:

The amino acid in Fischer projection and interpret it as D- or L- enantiomer.

Concept introduction:

Fischer projections are the representation of bonds by using horizontal and vertical lines in the 3D state. The horizontal lines represent the bonds that are out of paper towards the vision and the vertical lines represent the bonds pointing out the back of the paper away from vision. The intersection between the two lines represents the carbon atom.

A carbon which has all the four different atoms or group of atoms has tetrahedral geometry and such carbon molecule is referred to as the chiral carbon. The two different forms in which a single chiral center can exist is referred to as enantiomers. Simply, the substances which show optical isomerism exist as two isomers known as enantiomers. Enantiomers are non-super imposable mirror images of each other. The number of enantiomers of a molecule depends on the number of chiral centers.

Pictorial representation:

The Fischer projection of glutamine is represented as below:

Fig. 3(a): Fischer projection of glutamine.

Answer 12

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Ch. 5 - Prob. 1P Ch. 5 - Draw the structure of the peptide DTLH, showing...Ch. 5 - Prob. 3P Ch. 5 - Prob. 4P Ch. 5 - Prob. 5P Ch. 5 - Prob. 6P Ch. 5 - Prob. 7P Ch. 5 - Given the following peptide SEPIMAPVEYPK a....Ch. 5 - A mutant form of polypeptide hormone angiotensin...Ch. 5 - Prob. 10P

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