Concept explainers
(a)
Interpretation:
The structure of all the
Concept introduction:
The simple sugars are monosaccharides having five or six carbon atoms as in fructose and glucose. At carbon
(b)
Interpretation:
The structure of an achiral ketopentose
Concept introduction:
A carbon atom is said to be chiral when all four atoms attached to it are different. It is also known as asymmetric carbon atom. Similarly when a molecule cannot be divided into two similar parts it is known as chiral or asymmetrical. When a molecule has a plane of symmetry, it is considered to be achiral. It means that molecule can be divided into two equal parts through the plane of symmetry.
(c)
Interpretation:
The structure of
Concept introduction:
Two isomers have same formula but different structures. In case of sugars, two isomers are possible on the basis of functional group present in the molecule. In pentose and hexose sugar they may be open ring structure with aldehyde group or close ring structures with keto group as main functional groups (keto, aldo isomers).
(d)
Interpretation:
The structure of
Concept introduction: Two isomers have same chemical formula but different structures. In case of sugars two isomers are possible on the basis of functional group present.( They may be open ring with aldehyde or close ring with keto group as their functional group.
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Organic Chemistry
- What product or products are obtained when d-galactose reacts with each of the following? a. nitric acid + ∆ b. Ag+, NH3, HO- c. NaBH4, followed by H3O+ d. excess CH3I + Ag2O e. Br2 in water f. ethanol + HClg. 1. hydroxylamine/trace acid 2. acetic anhydride/∆ 3. HO-/H2Oarrow_forwardDraw the products formed when cholesterol is treated with each reagent. Indicate the stereochemistry around anystereogenic centers in the product.a. CH3COCIb. H2, Pd-Cc. PCCd. leic acid, H+e. [1] BH3 ·THF; [2] H2O2, -OHarrow_forwardDraw 4-O(beta-D-glucopyranosyl)-alpha-D-glucopyranosearrow_forward
- Write down the reactions: D-Glucopyranose + (CH3CO)2 O →arrow_forwardDraw Fischer projections for the product(s) formed by reaction of d-ribose with the following. In addition, state whether each product is optically active or inactive Q. C6H5NH2arrow_forwardd-Glucose most often exists as a pyranose, but it can also exist as a furanose. Draw the Haworth projection of a-d-glucofuranose.arrow_forward
- Predict the products obtained when d-galactose reacts with each reagent.(a) Br2 and H2O (b) NaOH, H2O (c) CH3OH, H +arrow_forwardIdentify the sugar in each description. a. An aldopentose that is not d-arabinose forms d-arabinitol when it is reduced with NaBH4. b. A sugar that is not D-altrose forms d-altraric acid when it is oxidized with nitric acid. c. A ketose that, when reduced with NaBH4, forms d-altritol and d-allitol.arrow_forwardWhat is the function of lyases? a. to catalyze redox reactions b. They catalyze reactions in which H₂O, NH3 and CO2 groups are removed c. They catalyze hydrolysis reactions. D. transfer active groupsarrow_forward
- Which statements are correct regarding the formation of maltose?A. Hydrolysis reaction between alpha-D-glucose and beta-D-glucoseB. Condensation reaction between alpha-D-glucose and beta-D-glucoseC. Condensation reaction between beta-galactose and beta-glucoseD. Hydrolysis of starch into a di-saccharide product a). A and B b). C and D c). B and D d). B and C e). B, C and Darrow_forwardDraw the product that is obtained from the reaction of cholesterol with the following reagents a. H2, Pd/C b. acetyl chloride c. H2SO4, ∆ d. H2O, H+ e. a peroxyacidarrow_forwardWhat products would be formed if CH3CH2CHOHCH(CH3)2 is dehydrated?arrow_forward
- Introduction to General, Organic and BiochemistryChemistryISBN:9781285869759Author:Frederick A. Bettelheim, William H. Brown, Mary K. Campbell, Shawn O. Farrell, Omar TorresPublisher:Cengage Learning