Practice Questions

The blue color formed in the iodine test for starch is due to a charge-transfer complex. This test will yield a negative result (no blue color) with a sample of glycogen because glycogen’s

A. Lower molecular weight prevents complex formation
B. Much shorter average chain length of its outer branches forms an unstable, reddish-brown complex
C. Absence of α-1,4 linkages prevents iodine binding
D. Covalent linkage to proteins blocks the iodine-binding sites

The iodine test requires a helix of sufficient length to stabilize the polyiodide chain. Glycogen's highly branched structure means its α-1,4 helical segments are very short. With iodine, it yields a reddish-brown color (not blue-black), which can be easily confused with a negative test if not careful.

nmdcat.online BIO NMDCAT
Jun 27, 2026

Regarding the solubility of monosaccharides, they are highly soluble in water due to their

A. Non-polar hydrocarbon chains
B. High molecular weight
C. Numerous hydroxyl groups that form hydrogen bonds with water
D. Furanose ring structure

Each monosaccharide has several polar -OH groups that can participate in hydrogen bonding with water molecules. This strong interaction (adhesion) overcomes the sugar-sugar interactions and allows the sugars to dissolve readily in water.

nmdcat.online BIO NMDCAT
Jun 27, 2026

The D/L designation is fixed by the configuration of the highest-numbered chiral center (C-5 in hexoses). The α and β anomers are defined specifically by the orientation of the hydroxyl group on the newly formed chiral center, the anomeric carbon (C-1 in aldoses), relative to the ring.

nmdcat.online BIO NMDCAT
Jun 27, 2026

Amylopectin is a homopolymer of D-glucose. Complete hydrolysis with strong acid will break all the α-1,4 and α-1,6 glycosidic bonds, yielding only D-glucose monomers as the final product.

nmdcat.online BIO NMDCAT
Jun 27, 2026

The phenomenon of “resistant starch” refers to starch and starch degradation products that

A. Are completely hydrolyzed in the mouth by salivary amylase
B. Escape digestion in the small intestine and are fermented in the large intestine
C. Inhibit the action of pancreatic lipase
D. Are covalently bonded to cellulose, making them indigestible

Resistant starch is physically inaccessible or structurally resistant to pancreatic amylases. It passes to the colon, where it acts similarly to soluble fiber, being fermented by gut microbiota, producing beneficial short-chain fatty acids.

nmdcat.online BIO NMDCAT
Jun 27, 2026

The glycosidic linkage of the polysaccharide agar, extracted from red algae, is composed of D-galactose and an unusual L-galactose derivative. The primary biological application of agar in a laboratory setting is based on its property of

A. Being a highly digestible nutrient for bacterial growth
B. Forming a stable, inert gel that solidifies at a temperature below the growth optimum of most microorganisms
C. Inhibiting the growth of fungi while allowing bacterial growth
D. Acting as a reducing agent in biochemical assays

Agar melts at ~85°C and solidifies at ~32-40°C. Once gelled, it remains solid at typical incubation temperatures (e.g., 37°C) and is resistant to degradation by most microorganisms, making it an ideal, inert solidifying agent for culture media.

nmdcat.online BIO NMDCAT
Jun 27, 2026

A comparison of the open-chain forms of glucose and fructose reveals that they are

A. Enantiomers
B. Structural isomers
C. Diastereomers
D. Anomers

Both have the same molecular formula (C₆H₁₂O₆), but different functional groups—glucose is an aldehyde (aldose) and fructose is a ketone (ketose). This difference in the connectivity of atoms makes them structural (constitutional) isomers.

nmdcat.online BIO NMDCAT
Jun 27, 2026

In plants, the formation of starch granules involves the coordinated action of starch synthase (for α-1,4 chain extension) and branching enzyme. The branching enzyme creates α-1,6 linkages by

A. Hydrolyzing an α-1,4 bond and then re-forming an α-1,6 bond with a different sugar
B. Cleaving a short α-1,4-linked oligosaccharide chain from one location and transferring it to the C-6 hydroxyl of a glucose in another chain
C. Activating glucose with UTP and then linking it to a C-6 hydroxyl
D. Phosphorylating the C-6 position to make it susceptible to nucleophilic attack

Branching enzyme is a transglycosylase. It cuts a short α-1,4-linked chain of 6-7 glucose units and transfers it to the 6-OH position of a glucose residue in the same or a nearby chain. This creates the α-1,6 branch points characteristic of amylopectin and glycogen.

nmdcat.online BIO NMDCAT
Jun 27, 2026

Rumen microbes ferment cellulose and other carbohydrates to volatile fatty acids (VFAs) like acetate, propionate, and butyrate. These are absorbed through the rumen wall and serve as the primary energy source for the ruminant, not the glucose monomers of cellulose.

nmdcat.online BIO NMDCAT
Jun 27, 2026

The Lobry de Bruyn–Alberta van Ekenstein transformation proceeds through the removal of a proton from C-2, forming an enediol (or enolate) intermediate. This intermediate can reprotonate to give either the original aldose (glucose), its C-2 epimer (mannose), or the ketose (fructose).

nmdcat.online BIO NMDCAT
Jun 27, 2026
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