A disaccharide X cannot be oxidised by bromine water. The acid hydrolysis of X leads to a laevorotatory solution. The disaccharide X is
Sucrose is a non-reducing disaccharide composed of glucose and fructose units joined together by a glycosidic bond. It cannot be oxidized by bromine water because it does not have a reducing group (such as an aldehyde or a ketone) that can be oxidized.
When sucrose undergoes acid hydrolysis, it breaks down into its constituent monosaccharides, glucose, and fructose. This hydrolysis reaction occurs due to the cleavage of the glycosidic bond. The resulting mixture of glucose and fructose is known as invert sugar and it is laevorotatory, meaning it rotates plane-polarized light to the left.
Therefore, the disaccharide X is most likely sucrose.
List-I | List-II | ||
(A) | 1 mol of H2O to O2 | (I) | 3F |
(B) | 1 mol of MnO-4 to Mn2+ | (II) | 2F |
(C) | 1.5 mol of Ca from molten CaCl2 | (III) | 1F |
(D) | 1 mol of FeO to Fe2O3 | (IV) | 5F |
List-I | List-II | ||
(A) | [Co(NH3)5(NO2)]Cl2 | (I) | Solvate isomerism |
(B) | [Co(NH3)5(SO4)]Br | (II) | Linkage isomerism |
(C) | [Co(NH3)6] [Cr(CN)6] | (III) | Ionization isomerism |
(D) | [Co(H2O)6]Cl3 | (IV) | Coordination isomerism |
Organic Chemistry is a subset of chemistry dealing with compounds of carbon. Therefore, we can say that Organic chemistry is the chemistry of carbon compounds and is 200-225 years old. Carbon forms bond with itself to form long chains of hydrocarbons, e.g.CH4, methane and CH3-CH3 ethane. Carbon has the ability to form carbon-carbon bonds quite elaborately. Polymers like polyethylene is a linear chain where hundreds of CH2 are linked together.
Read Also: Organic Compounds
Organic chemistry is applicable in a variety of areas including-