Hydroxyl groups are found in all monosaccharides along with a carbonxyl on the first or second carbon.
A kenopentose has a ketone functional group attatched to a monosaccharide that contains all hydroxyl functional groups.
They're polar
The actual triglyceride doesn't have any functional groups. They have all been used during the making of the triglyceride. There used to be 3 hydroxyl functional groups on the glycerol backbone, and 3 carboxylic acid functional groups (1 each on the three fatty acids). However, after the fatty acids react (become esterified) with the alcoholic groups on glycerol, there are no more functional groups in the triglyceride.
Monosaccharides are classified by the number of carbon atoms and the types of functional groups present in the sugar. For example, glucose and fructose have the same chemical formula (C6H12O6), but a different structure: glucose having an aldehyde (internal hydroxyl shown as: -OH) and fructose having a keto group (internal double-bond O, shown as: =O). This functional group difference, as small as it seems, accounts for the greater sweetness of fructose as compared to glucose.
Attached to all straight chain forms of monosaccharides are side groups. The side groups are one carbonyl functional group and one hydroxyl group on the remaining carbon atoms.
A kenopentose has a ketone functional group attatched to a monosaccharide that contains all hydroxyl functional groups.
They're polar
The actual triglyceride doesn't have any functional groups. They have all been used during the making of the triglyceride. There used to be 3 hydroxyl functional groups on the glycerol backbone, and 3 carboxylic acid functional groups (1 each on the three fatty acids). However, after the fatty acids react (become esterified) with the alcoholic groups on glycerol, there are no more functional groups in the triglyceride.
Monosaccharides are classified by the number of carbon atoms and the types of functional groups present in the sugar. For example, glucose and fructose have the same chemical formula (C6H12O6), but a different structure: glucose having an aldehyde (internal hydroxyl shown as: -OH) and fructose having a keto group (internal double-bond O, shown as: =O). This functional group difference, as small as it seems, accounts for the greater sweetness of fructose as compared to glucose.
If you mean the hydroxyl functional group (-OH), then only serine and threonine contain it. However, all amino acids contain one or more carboxylic acid (-COOH) functional groups and they all contain OH as part of that functional group, though the carboxylic acid functional group should be considered a single unit.
galactose and fructose
Attached to all straight chain forms of monosaccharides are side groups. The side groups are one carbonyl functional group and one hydroxyl group on the remaining carbon atoms.
Nationality groups found were Anglo-Saxon, British, and Protestants. These were found in all the colonies.
Amino acids are of different types e.g. acidic,basic,neutral, imino ,and sulpher containing etc but all types of amino acids possess two functional groups. These functional groups are amino group and carboxylicgroup. An amino group is chemically NH2 , it is a basic group. Other functional group is carboxylic group which is chemically COOH , it is acidic in nature, Functional group is part of molecule that gives it ,its specific chemical characters.Presence of these groups makes amino acid amphoteric.
The functional group that contains nitrogen is carbonyl, also known as C=O. Out of all of the carbonyl groups, amides are considered the most stable.
Two functional groups are found in all amino acids. These functional groups are the amino group (-NH2) and the carboxyl group (-COOH). The hydrogen atom of the carboxyl group can be broken off quite easily; this gives amino acids their acidic properties.
No they can not be found on all amino acids that is a false statement