(a) Interpretation: The α anomer of given aldohexose by the use of Haworth projection is to be drawn. Concept introduction: The structural representation of sugar molecule in cyclic form is known as Haworth projection. A compound in which the hydroxyl group of first and sixth carbon atom is on the same side is known as β anomer, otherwise α anomer.

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Answer 1

Question

Chapter 26.6, Problem 12P

Interpretation Introduction

(a)

Interpretation: The α anomer of given aldohexose by the use of Haworth projection is to be drawn.

Concept introduction: The structural representation of sugar molecule in cyclic form is known as Haworth projection. A compound in which the hydroxyl group of first and sixth carbon atom is on the same side is known as β anomer, otherwise α anomer.

Interpretation Introduction

(b)

Interpretation: The α anomer of given aldohexose by the use of Haworth projection is to be drawn.

Concept introduction: The structural representation of sugar molecule in cyclic form is known as Haworth projection. A compound in which the hydroxyl group of first and sixth carbon atom is on the same side is known as β anomer, otherwise α anomer.

Interpretation Introduction

(c)

Interpretation: The β anomer of given aldohexose by the use of Haworth projection is to be drawn.

Concept introduction: The structural representation of sugar molecule in cyclic form is known as Haworth projection. A compound in which the hydroxyl group of first and sixth carbon atom is on the same side is known as β anomer, otherwise α anomer.

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1. Calculate the accurate monoisotopic mass (using all 1H, 12C, 14N, 160 and 35CI) for your product using the table in your lab manual. Don't include the Cl, since you should only have [M+H]*. Compare this to the value you see on the LC-MS printout. How much different are they? 2. There are four isotopic peaks for the [M+H]* ion at m/z 240, 241, 242 and 243. For one point of extra credit, explain what each of these is and why they are present. 3. There is a fragment ion at m/z 184. For one point of extra credit, identify this fragment and confirm by calculating the accurate monoisotopic mass. 4. The UV spectrum is also at the bottom of your printout. For one point of extra credit, look up the UV spectrum of bupropion on Google Images and compare to your spectrum. Do they match? Cite your source. 5. For most of you, there will be a second chromatographic peak whose m/z is 74 (to a round number). For one point of extra credit, see if you can identify this molecule as well and confirm by…

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can you draw each step on a piece of a paper please this is very confusing to me

Answer 2

Question

Chapter 26.6, Problem 12P

Interpretation Introduction

(a)

Interpretation: The α anomer of given aldohexose by the use of Haworth projection is to be drawn.

Concept introduction: The structural representation of sugar molecule in cyclic form is known as Haworth projection. A compound in which the hydroxyl group of first and sixth carbon atom is on the same side is known as β anomer, otherwise α anomer.

Interpretation Introduction

(b)

Interpretation: The α anomer of given aldohexose by the use of Haworth projection is to be drawn.

Concept introduction: The structural representation of sugar molecule in cyclic form is known as Haworth projection. A compound in which the hydroxyl group of first and sixth carbon atom is on the same side is known as β anomer, otherwise α anomer.

Interpretation Introduction

(c)

Interpretation: The β anomer of given aldohexose by the use of Haworth projection is to be drawn.

Concept introduction: The structural representation of sugar molecule in cyclic form is known as Haworth projection. A compound in which the hydroxyl group of first and sixth carbon atom is on the same side is known as β anomer, otherwise α anomer.

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Answer 3

Question

Chapter 26.6, Problem 12P

Interpretation Introduction

(a)

Interpretation: The α anomer of given aldohexose by the use of Haworth projection is to be drawn.

Concept introduction: The structural representation of sugar molecule in cyclic form is known as Haworth projection. A compound in which the hydroxyl group of first and sixth carbon atom is on the same side is known as β anomer, otherwise α anomer.

Interpretation Introduction

(b)

Interpretation: The α anomer of given aldohexose by the use of Haworth projection is to be drawn.

Concept introduction: The structural representation of sugar molecule in cyclic form is known as Haworth projection. A compound in which the hydroxyl group of first and sixth carbon atom is on the same side is known as β anomer, otherwise α anomer.

Interpretation Introduction

(c)

Interpretation: The β anomer of given aldohexose by the use of Haworth projection is to be drawn.

Concept introduction: The structural representation of sugar molecule in cyclic form is known as Haworth projection. A compound in which the hydroxyl group of first and sixth carbon atom is on the same side is known as β anomer, otherwise α anomer.

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Answer 4

Question

Chapter 26.6, Problem 12P

Interpretation Introduction

(a)

Interpretation: The α anomer of given aldohexose by the use of Haworth projection is to be drawn.

Concept introduction: The structural representation of sugar molecule in cyclic form is known as Haworth projection. A compound in which the hydroxyl group of first and sixth carbon atom is on the same side is known as β anomer, otherwise α anomer.

Interpretation Introduction

(b)

Interpretation: The α anomer of given aldohexose by the use of Haworth projection is to be drawn.

Concept introduction: The structural representation of sugar molecule in cyclic form is known as Haworth projection. A compound in which the hydroxyl group of first and sixth carbon atom is on the same side is known as β anomer, otherwise α anomer.

Interpretation Introduction

(c)

Interpretation: The β anomer of given aldohexose by the use of Haworth projection is to be drawn.

Concept introduction: The structural representation of sugar molecule in cyclic form is known as Haworth projection. A compound in which the hydroxyl group of first and sixth carbon atom is on the same side is known as β anomer, otherwise α anomer.

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Answer 5

Chapter 26.6, Problem 12P

Interpretation Introduction

(a)

Interpretation: The α anomer of given aldohexose by the use of Haworth projection is to be drawn.

Concept introduction: The structural representation of sugar molecule in cyclic form is known as Haworth projection. A compound in which the hydroxyl group of first and sixth carbon atom is on the same side is known as β anomer, otherwise α anomer.

Interpretation Introduction

(b)

Interpretation: The α anomer of given aldohexose by the use of Haworth projection is to be drawn.

Concept introduction: The structural representation of sugar molecule in cyclic form is known as Haworth projection. A compound in which the hydroxyl group of first and sixth carbon atom is on the same side is known as β anomer, otherwise α anomer.

Interpretation Introduction

(c)

Interpretation: The β anomer of given aldohexose by the use of Haworth projection is to be drawn.

Concept introduction: The structural representation of sugar molecule in cyclic form is known as Haworth projection. A compound in which the hydroxyl group of first and sixth carbon atom is on the same side is known as β anomer, otherwise α anomer.

Answer 6

Chapter 26.6, Problem 12P

Interpretation Introduction

(a)

Interpretation: The α anomer of given aldohexose by the use of Haworth projection is to be drawn.

Concept introduction: The structural representation of sugar molecule in cyclic form is known as Haworth projection. A compound in which the hydroxyl group of first and sixth carbon atom is on the same side is known as β anomer, otherwise α anomer.

Answer 7

Chapter 26.6, Problem 12P

Interpretation Introduction

(a)

Interpretation: The α anomer of given aldohexose by the use of Haworth projection is to be drawn.

Concept introduction: The structural representation of sugar molecule in cyclic form is known as Haworth projection. A compound in which the hydroxyl group of first and sixth carbon atom is on the same side is known as β anomer, otherwise α anomer.

Answer 8

Interpretation Introduction

(b)

Interpretation: The α anomer of given aldohexose by the use of Haworth projection is to be drawn.

Concept introduction: The structural representation of sugar molecule in cyclic form is known as Haworth projection. A compound in which the hydroxyl group of first and sixth carbon atom is on the same side is known as β anomer, otherwise α anomer.

Answer 9

Interpretation Introduction

(b)

Interpretation: The α anomer of given aldohexose by the use of Haworth projection is to be drawn.

Concept introduction: The structural representation of sugar molecule in cyclic form is known as Haworth projection. A compound in which the hydroxyl group of first and sixth carbon atom is on the same side is known as β anomer, otherwise α anomer.

Answer 10

Interpretation Introduction

(c)

Interpretation: The β anomer of given aldohexose by the use of Haworth projection is to be drawn.

Concept introduction: The structural representation of sugar molecule in cyclic form is known as Haworth projection. A compound in which the hydroxyl group of first and sixth carbon atom is on the same side is known as β anomer, otherwise α anomer.

Answer 11

Interpretation Introduction

(c)

Interpretation: The β anomer of given aldohexose by the use of Haworth projection is to be drawn.

Concept introduction: The structural representation of sugar molecule in cyclic form is known as Haworth projection. A compound in which the hydroxyl group of first and sixth carbon atom is on the same side is known as β anomer, otherwise α anomer.

Answer 12

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Answer 13

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Answer 14

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Answer 15

Ch. 26.2 - Prob. 1P Ch. 26.2 - Prob. 2P Ch. 26.2 - Label each stereogenic center as R or S. a. b. c....Ch. 26.2 - Convert the ball-and-stick model to a Fischer...Ch. 26.2 - Prob. 5P Ch. 26.2 - Prob. 6P Ch. 26.3 - Prob. 7P Ch. 26.3 - Prob. 8P Ch. 26.4 - Prob. 9P Ch. 26.4 - Prob. 10P

Solution Summary: The author explains how the anomer of given aldohexose is drawn by the use of Haworth projection.

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Chapter 26 Solutions