Yes, since galactose is a monosaccharide it can undergo mutarotaion just like glucose. The only difference between glucose and galactose is the side the OH and H are on, on the carbon atom #4.
When galactose becomes a in chain form, drawn in Fischer formula the OH will be on the left side instead of the right side.
This is how you get Galactose α or β, at the end of the mutarotation the chain can link back into a ring either way, α with the carbon #1's OH on the bottom and H on top, or β with the OH on top and H on the bottom (Haworth formula).
no, because it is a nonreducing sugar. A reducing sugar has a hemiacetal on it's anomeric carbon, which always undergoes mutarotation.
no
Mutarotation and it importance in carbohydrate in biochemistry
No, raffinose is not capable of mutarotation. It is a trisaccharide consisting of galactose, glucose and fructose monomers connected by glycosidic bonds. The glycosidic bonds lock the three rings in their cyclic forms making it so that mutarotation will not be possible.
yes it is a reducing sugar, it has a free anomeric OH group. thus it can also mutarotate
Alkanes like (methane, ethane, propane etc.) … They do not undergo addition reactions
They undergo similar reactions because they are both in the same group on the periodic table.
Mutarotation and it importance in carbohydrate in biochemistry
a reducung sugar since it has an aldehyde group
Yes
No, raffinose is not capable of mutarotation. It is a trisaccharide consisting of galactose, glucose and fructose monomers connected by glycosidic bonds. The glycosidic bonds lock the three rings in their cyclic forms making it so that mutarotation will not be possible.
yes it is a reducing sugar, it has a free anomeric OH group. thus it can also mutarotate
of Undergo, imp. of Undergo.
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He will undergo surgery in the morning.We all have to undergo these examinations.
Undergo is a verb.
of Undergo, imp. of Undergo.
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no they undergo mitosis