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. Unlike reducing sugars, sucrose cannot be oxidized by bromine water because it does not have a reducing group (such as an aldehyde or a ketone) that can undergo oxidation.
When sucrose undergoes acid hydrolysis, it breaks down into its constituent monosaccharides, glucose and fructose. This process occurs due to the cleavage of the glycosidic bond between the two monosaccharides. The resulting mixture of glucose and fructose is known as invert sugar.
Invert sugar is laevorotatory, meaning it rotates plane-polarized light to the left. This property arises from the combination of glucose and fructose, which in their free form have optical activities that are not completely canceled out.
Based on the information provided, the disaccharide X is most likely sucrose.
The major products obtained from the reactions in List-II are the reactants for the named reactions mentioned in List-I. Match each entry in List-I with the appropriate entry in List-II and choose the correct option.
The reaction sequence given below is carried out with 16 moles of X. The yield of the major product in each step is given below the product in parentheses. The amount (in grams) of S produced is ____.
Use: Atomic mass (in amu): H = 1, C = 12, O = 16, Br = 80
Two identical concave mirrors each of focal length $ f $ are facing each other as shown. A glass slab of thickness $ t $ and refractive index $ n_0 $ is placed equidistant from both mirrors on the principal axis. A monochromatic point source $ S $ is placed at the center of the slab. For the image to be formed on $ S $ itself, which of the following distances between the two mirrors is/are correct:
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-