The School of Biomedical Sciences Wiki - User contributions [en]

Free radical

2018-12-06T18:42:40Z

180639632: Created page with "An uncharged molecule with an unpaired electron, making it highly reactive."

An uncharged molecule with an unpaired [[Electron|electron]], making it highly reactive.

Vestigial

2018-12-06T18:40:57Z

180639632: Created page with "Vestigial describes an organ or body part that continues to exist without retaining its original function. An example of this is the appendix in humans."

Vestigial describes an [[organ |organ]] or body part that continues to exist without retaining its original function. An example of this is the appendix in humans.

Chromosome 17

2018-12-06T18:36:51Z

180639632:

Chromosome 17 is one of the 23 pairs of [[Chromosome|chromosomes]] in [[Human|humans]], people normally have two copies of this chromosome. [[Image:Chromosome 17.png]]

Chromosome 17

2018-12-06T18:36:07Z

180639632: Created page with "Chromosome 17 is one of the 23 pairs of chromosomes in humans, people normally have two copies of this chromosome. Image:Chromosome_17.png"

Chromosome 17 is one of the 23 pairs of chromosomes in humans, people normally have two copies of this chromosome. [[Image:Chromosome_17.png]]

File:Chromosome 17.png

2018-12-06T18:34:45Z

180639632: Chromosome 17 highlighted in red.

Chromosome 17 highlighted in red.

D-form

2018-12-06T18:18:49Z

180639632:

D - form [[Sugars|sugars]] have the -OH [[Functional_group|functional group]] facing to the right on the furthest [[Chiral centre|chiral centre]] down on the [[Fischer Projection|Fischer Projection]] structure of the sugar.

D - form configurations are most common in sugars.

It is called D-form because of the direction in which the sugar rotates in the plane of [[Polarised_light|polarized light]], hence to the right it is called dextrorotatory (D).

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  [[Image:DL-Glucose svg.png|194x157px|DL-Glucose svg.png]]

D-form

2018-12-06T18:17:12Z

180639632:

D - form [[Sugars|sugars]] have the -OH functional group facing to the right on the furthest [[Chiral centre|chiral centre]] down on the [[Fischer Projection|Fischer Projection]] structure of the sugar.

D - form configurations are most common in sugars.

It is called D-form because of the direction in which the sugar rotates in the plane of polarized light, hence to the right it is called dextrorotatory (D).

  [[Image:DL-Glucose svg.png|194x157px|DL-Glucose svg.png]]

D-form

2018-12-06T18:11:47Z

180639632:

File:DL-Glucose svg.png

2018-12-06T08:47:35Z

180639632:

[[D-form]]

File:DL-Glucose svg.png

2018-12-06T08:42:16Z

180639632:

D-form

2018-12-05T09:53:20Z

180639632: Created page with "D - form sugars have the -OH functional group facing to the right on the furthest chiral centre down on the Fischer Projection structure of the sugar. D - form configurations a..."

D - form sugars have the -OH functional group facing to the right on the furthest chiral centre down on the Fischer Projection structure of the sugar.

D - form configurations are most common in sugars.