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6 votes
2 answers
161 views

What does ‘D’ in GADP (glyceraldehyde 3-phosphate) stand for?

Wikipedia says glyceraldehyde-3-phosphate can be abbreviated as G3P, GA3P, GADP, GAP, TP, GALP or PGAL, and many resources seem to use GADP as its abbreviation. I have no idea where ‘D’ came from. ...
chrononaute's user avatar
0 votes
0 answers
27 views

Why can't the fructose monomer in sucrose be α-fructose?

In all academic sources, sucrose is identified as α−glucose (1-->2) β−fructose. However, I cannot find any explanation anywhere as to why the fructose monomer has to be in the β configuration. ...
MD P's user avatar
  • 11
0 votes
0 answers
24 views

Bioplastic from starch

I am doing research in bioplastic from starch. I have tried many quantities and concentrations of starch, vinegar and glycerol at different temperatures. But I am unable to get a certain result of the ...
Maneeha. Ajmal's user avatar
0 votes
0 answers
263 views

Why does glucose react with hydroxyl amine and HCN but doesn't give Schiff's test or react with NaHSO3?

I can't understand this because if there isn't a free CHO group then it also shouldn't react with NH2OH and HCN. On the same note can anyone also explain why pentaacetate of glucose not react with ...
Tanush Gupta's user avatar
-1 votes
2 answers
2k views

Are Starch, Amylose and, Amylopectin reducing sugars?

Amylose and Amylopectin; As per the information I've learnt, Amylose is considered a reducing sugar but Amylopectin is not because Amylose has a free "reducing end" which Amylopectin lacks, ...
pointlessHumility01's user avatar
1 vote
2 answers
286 views

How does industry separate glucose from fructose using liquid chromatography when producing high-fructose corn syrup?

Can someone explain how the separation of glucose and fructose is achieved using liquid chromatography in the industrial production of high-fructose corn syrup? I've seen references to ion-exchange ...
vossman77's user avatar
  • 121
0 votes
1 answer
410 views

Does changes in pH affects cyclic form of glucose in water solution?

Glucose in water solution is mainly in cyclic form. Both base and acid can catalize formation of hemiacetal, but in distinct mechanisms. I found information that monosacharides eg. glucose exist ...
Krzysztof Dryjka's user avatar
10 votes
1 answer
1k views

Can sugars dissolve in liquid ammonia?

Can monosaccharides and disaccharides dissolve in liquid ammonia due to hydrogen bond formation? My rationale is that these sugars may be able to form hydrogen bond with ammonia ($\ce{NH3}$).
Soduthanthanakka's user avatar
0 votes
0 answers
2k views

Haworth structures of sucrose and lactose

The haworth structures of lactose and sucrose is My question is regarding the glyosidic linkage, in lactose it is represented as a zig zag and in sucrose it is a "V". What does that mean. ...
user avatar
2 votes
0 answers
212 views

Do enzymes that digest ᴅ-glucose react with ʟ-glucose?

ᴅ-Glucose is common in nature and ʟ-glucose is synthesized in the lab. I know that humans can't use ʟ-glucose in their aerobic pathways because it doesn't match the active site of the enzyme, but why ...
mojopinos's user avatar
7 votes
2 answers
3k views

Oxidation of hydroxyl groups of glucose

In all oxidation reactions of glucose, it seems that the aldehyde group alone gets oxidised and none of the hydroxyl groups. In one reaction with nitric acid, the aldehyde group and the terminal ...
Vat's user avatar
  • 103
1 vote
0 answers
449 views

Where does the beta notation come from in the alpha 1,2 beta glycosidic bond (in sucrose)? [duplicate]

I am confused as to where the beta is coming from (in the alpha-1,2-beta glycosidic bond in sucrose). I understand that the alpha is from the anomeric carbon of the glucose, but I don't see how the ...
Huzaifah Masood's user avatar
8 votes
1 answer
2k views

Does cooling a potato change the nature of its carbohydrates?

A talk-show guest of Joe Rogan claimed that cooling a potato after cooking creates "resistant starch" that's better for human consumption https://www.youtube.com/watch?v=niwqfwA2Lb8 The ...
MWB's user avatar
  • 519
3 votes
1 answer
3k views

How are glycosidic linkages formed?

Consider glycosidic linkages in disaccharides. I know a condensation reaction occurs, with the loss of water. But which OH is lost? The O in the linkage belongs to which monosaccharide? Example: ...
user226375's user avatar
5 votes
2 answers
3k views

How does existence of alpha and beta form of glucose prove that it exists as a cyclic structure

My book says that Glucose is found to exist in two different crystalline forms which are named as $\alpha$ and $\beta$. Next it says that This behaviour could not be explained by the open ...
Eagle's user avatar
  • 305
3 votes
1 answer
228 views

Production of ʟ-glucose

What chain(s) of reactions are used to produce ʟ-glucose? I did a search on Google Scholar, but to my surprise nothing came up. My guess would be that the synthesis starts from ᴅ-glucose for which ...
frapadingue's user avatar
3 votes
1 answer
89 views

Can Molisch test be used to separate monosaccharides from polysaccharides?

Do the results of Molisch test on monosaccharides have any differences with when it's done to disaccharides or polysaccharides?
Aury's user avatar
  • 55
3 votes
1 answer
12k views

Why can't amylase digest glycogen?

Amylase is an enzyme that breaks down starch in the form of amylopectin and amylose. Both amylose and amylopectin are formed by alpha glucose joined together by (1-4) and (1-6) glycosidic bonds. ...
user35897's user avatar
  • 131
3 votes
1 answer
12k views

Monosaccharides configurations (alpha beta, D L) identification

I am really finding it difficult to identify the correct configuration(s) of a given monosaccharide, in fact my friends and I have been trying to solve this, much to our annoyance. In one of our ...
Nemexia's user avatar
  • 167
6 votes
4 answers
4k views

Why is fermentation of cellulose to produce biofuel and nutrients so difficult?

The formula for glucose is $\ce{C6H12O6}$ and that of cellulose is very similar $\ce{C6H10O5}$. Glucose can be readily fermented by yeast and other micro-organisms to produce carbon dioxide and ...
0tyranny0poverty's user avatar
10 votes
1 answer
432 views

What is the correct way to notate conformation preferences of polysaccharides?

In some webpages (1 or 2) are found the way to notate the conformational preferences of monosaccharides such as furanose and pyranose. But, it lacks to give a brief description on how to do it with ...
Another.Chemist's user avatar
0 votes
1 answer
705 views

Glycoside Formation Reaction

Whenever we add $\ce{H+}$/ Ethanol to glucose in its hemiacetal form, why doesn't pinacone/pinacolone rearrangement take place in place of nucleophillic substitution. The product would lead to ...
Ayushmaan's user avatar
  • 1,132
0 votes
1 answer
178 views

Asking about definitions of word "sugar" in biochemistry

In a lecture about anabolic pathways of sugar, the lecturer was not clear when stating the name of a multiple sugar carrier & it sounded like "dolichol"so is it correct?
Marina Medhat's user avatar
9 votes
3 answers
27k views

How do you recognize a carbohydrate molecule?

I am studying carbohydrates in organic chemistry and I am confused a bit on what they are and how you recognize whether a molecule is a carbohydrate or not. For example, will a carbohydrate always ...
TLo's user avatar
  • 1,096
3 votes
2 answers
7k views

If α-glucose is less stable than β-glucose, why is glucose almost always α in its compounds?

Maltose, saccharose, turanose, trehalose, trehalulose, amylopectin, amylose - they are all α. Why? Also, why is cellulose β?
waterlemon's user avatar
  • 1,651
-4 votes
2 answers
17k views

In Glucose, how will you prove the presence of the following? [closed]

One carbonyl group 5 hydroxyl groups One primary alcholic group
Dev Aggarwal's user avatar
-2 votes
1 answer
746 views

Why isn't sucrose a reducing sugar but maltose is? [duplicate]

I read one of the answers for a similar question, According to that it is due to the hemiacetale group converting into a carbonyl group. I don't get why the same thing can't be applied to sucrose ...
shihitzuuu's user avatar
0 votes
1 answer
212 views

Why does the AraC arabinose sensing system only respond to the presence of L-arabinose?

I understand that when arabinose is present it interacts with araC and changes it shape, promoting the binding of RNA polymerase with the promoter and GFP is produced. However, I don't understand why ...
J.Se's user avatar
  • 397
5 votes
1 answer
213 views

Polysaccharides from non-cyclic sugars?

I have only come across polysaccharides from monosaccharides that has undergone intramolecular cyclization reaction. I was wondering if it is possible for polysaccharides to form from linear sugars? ...
Meep's user avatar
  • 1,697
1 vote
0 answers
148 views

If Substance A is more soluble in water than Substance B, will Substance A be more easily absorbed by the body?

I am comparing the solubilities of artificial vs natural sweeteners for my Chemistry IB Internal Assessment. I must demonstrate personal engagement, so I am relating my topic to weight management in ...
IBstressed's user avatar
3 votes
1 answer
187 views

Gel filtration separation of cellulose, starch, oxytocin and palmitic acid

I am studying biochemistry and I have been asked by my teacher to find a procedure for separating cellulose, starch, the peptide oxytocin (9 a.a) and palmitic acid ($\ce{C16}$) using gel filtration ...
Unknown's user avatar
  • 140
1 vote
1 answer
650 views

Why do we have glycogen in the muscles and not glucose? [closed]

Why do we have glycogen in the muscles and not glucose? I know this is in contrast to liver cells, which, on demand, readily do break down their stored glycogen into glucose and send it through the ...
jowaher's user avatar
  • 11
4 votes
1 answer
3k views

Phosphoglucose isomerase mechanism

The mechanism for phosphoglucose isomerase changing glucose 6 phosphate to fructose 6 phosphate shows histidine protonating the c5 oxygen and lysine deprotonation the c1 oxygen to form an open chain ...
David's user avatar
  • 105
9 votes
1 answer
3k views

Why do polysaccharides consisting of alpha-glucose have helical structures?

Why do the polysaccharides consisting of alpha-glucose such as starch and glycogen have helical structure, while the one such as cellulose consisting of beta glucose don't display such structures? The ...
Snake's user avatar
  • 93
4 votes
1 answer
1k views

l- versus d-glucose

I recently purchased Dextrose from a local bulkfood store. I want to use it instead of table sugar. My concern is that it may be l-glucose instead of d-glucose. According to Wikipedia l-glucose is too ...
user8893's user avatar
3 votes
1 answer
2k views

Find the number of water molecules "embedded" in sucrose

Recently I got a question as follows: How many molecules of water are joined with 12 atoms of carbon in a molecule of sucrose ? (A) 12 (B) 11 (C) 6 (D) 10 I am unable to ...
Murtuza Vadharia's user avatar
1 vote
1 answer
326 views

Fermentation of different types of sugar

I'm searching for the difference in the fermentation of muscovado sugar, honey and sugar cane. I have used a specific microbiota to to ferment these three types of sugar and have to explain why I've ...
Silvia Torres's user avatar
29 votes
2 answers
82k views

Why does fructose reduce Tollen's reagent and Fehling's solution?

Even though fructose is a ketohexose (ketone-containing hexose, a six-carbon monosaccharide), it reduces Tollen's reagent and Fehling's solution. Generally, a ketone does not reduces Tollen's reagent ...
Nilay Ghosh's user avatar
  • 26.3k
2 votes
1 answer
89 views

Tensile properties of cellulose fibres

In cellulose fibres, such as cotton or hemp, I've noticed different percentages of lignin and cellulose. How does this affect their tensile strength and toughness? Are there any other important ...
chem293's user avatar
  • 21
3 votes
1 answer
298 views

Creating small amounts of cellulosic ethanol from bamboo

I own a medium-sized farm and commercial aquaponics business in Pennsylvania. I try to make my business as green, sustainable, carbon-neutral and self-sufficient as possible. As a way to cut out the ...
Calvin's user avatar
  • 31
14 votes
2 answers
5k views

Why starch (amylose) and cotton (cellulose) are so different?

Both amylose and cellulose have the same "monomer" structure (glucose), so what makes them look/form so differently?
Sparkler's user avatar
  • 4,265
6 votes
1 answer
564 views

How is it that fructose has a different metabolic pathway than glucose but yet glucose is converted to fructose?

Fructose is described to have a different metabolic pathway (a more fat-inducing one) than glucose (see: http://healthyeating.sfgate.com/difference-between-sucrose-glucose-fructose-8704.html) as it ...
Paze's user avatar
  • 703
14 votes
1 answer
61k views

How do you identify reducing / non-reducing sugar by looking at structure?

Identifying reducing / non-reducing sugar been confusing me for a while now , I know that reducing sugar contain aldehyde or ketone group . It's easy to identify them in monosaccharides but this ...
Heisenberg's user avatar
7 votes
2 answers
4k views

Can I break starch down into glucose units?

I was wondering if starch can be broken up into individual glucose units. Because on a site I saw, it said that through acid hydrolysis starch can be broken up into amylose and amylopectin. However, ...
ChapaPata's user avatar
2 votes
1 answer
6k views

In water, will sucrose be hydrolysed by water to form glucose and fructose molecules? [duplicate]

If I dissolve sucrose sugar ($\ce{C_12H_22O_11}$) in water, would the water readily hydrolyse the sucrose sugar to form glucose and fructose sugars?
krismath's user avatar
  • 483
4 votes
1 answer
237 views

Fermentation in beer (reaction schemes)?

I've been struggling with this for a while, and I can't seem to solve the problem. Alcohol is made in the fermentation process in beer: Sugars formed during mashing (maltose and maltotriose) will ...
Frederik Witte's user avatar
10 votes
2 answers
5k views

Is formaldehyde a carbohydrate?

Formaldehyde has the formula $\ce{CH2O}$, and the ratio of atoms in a simple carb is $\ce{1C:2H:1O}$. This fits the formula of carbohydrates. When I researched this, I found some sources saying that ...
Orcris's user avatar
  • 435