M2: Isomerism

20問 • 1年前

saoirse

通報

問題一覧

This is an optical isomer which rotates the beam of polarized light.

dextrorotatory

This is an optical isomer which rotates the beam of polarized light to the left.

levorotatory

This is used to measure the optical rotation molecules in solution.

polarimeter

The enantiomer with the OH group on the right (dextro) side of the chiral carbon farthest from the carbonyl group.

d enantiomer

The enantiomer with the OH group on the left (levo) side of the chiral carbon farthest from the carbonyl group.

l enantiomer

These are the most biologically active monosaccharides.

d isomers

These are naturally occuring enantiomers.

d enantiomers

These are unnaturally occuring enantiomers.

l enantiomers

In this anomer, the OH is written below the anomeric carbon.

alpha anomer

In this anomer, the OH is written above the anomeric carbon.

beta anomer

Our body can only utilize those of this anomers except in some cases, which is why most sugars are of this anomer:

alpha anomer

This places the anomeric carbon in C-1 and is obtained by cyclization of an aldehyde and an alcohol group.

pyranose

This places the anomeric carbon is C-2 and is obtained by cyclization of a ketone and an alcohol group.

furanose

This is the D-glucose in the liver by a specific enzyme.

epimerase

These are two sugars which differs from one another only in the configuration around a single carbon atom.

epimers

These are straight chain or open chain structures.

fischer projection

These are ring or cyclic structures; hemiacetals or hemiketals.

haworth projection

This is the product of the addition of an alcohol to the carbonyl group of an aldehyde.

hemiacetal

This is the product of the addition of an alcohol to the carbonyl group of a ketone.

hemiketal

These are projections of boat and chair structures.

newman projection

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Nature of Man

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Judaism

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Module 1: Introduction

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Module 1: Introduction

Module 2, Lesson 2

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Module 2, Lesson 1

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Module 2, Lesson 3

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M3: the cell

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M1: Biochemistry Introduction

M1: Water

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M2: Carbohydrates

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M2: Classification of Carbohydrates

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M2: Classification of Carbohydrates

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LIPIDS 2

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PROTEINS & AMINO ACIDS

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問題一覧

This is an optical isomer which rotates the beam of polarized light.

dextrorotatory

This is an optical isomer which rotates the beam of polarized light to the left.

levorotatory

This is used to measure the optical rotation molecules in solution.

polarimeter

The enantiomer with the OH group on the right (dextro) side of the chiral carbon farthest from the carbonyl group.

d enantiomer

The enantiomer with the OH group on the left (levo) side of the chiral carbon farthest from the carbonyl group.

l enantiomer

These are the most biologically active monosaccharides.

d isomers

These are naturally occuring enantiomers.

d enantiomers

These are unnaturally occuring enantiomers.

l enantiomers

In this anomer, the OH is written below the anomeric carbon.

alpha anomer

In this anomer, the OH is written above the anomeric carbon.

beta anomer

Our body can only utilize those of this anomers except in some cases, which is why most sugars are of this anomer:

alpha anomer

This places the anomeric carbon in C-1 and is obtained by cyclization of an aldehyde and an alcohol group.

pyranose

This places the anomeric carbon is C-2 and is obtained by cyclization of a ketone and an alcohol group.

furanose

This is the D-glucose in the liver by a specific enzyme.

epimerase

These are two sugars which differs from one another only in the configuration around a single carbon atom.

epimers

These are straight chain or open chain structures.

fischer projection

These are ring or cyclic structures; hemiacetals or hemiketals.

haworth projection

This is the product of the addition of an alcohol to the carbonyl group of an aldehyde.

hemiacetal

This is the product of the addition of an alcohol to the carbonyl group of a ketone.

hemiketal

These are projections of boat and chair structures.

newman projection