1. Sucrose undergoes hydrolysis to form an equimolar mixture of D-glucose and D-fructose, which has the opposite rotation of light compared to sucrose. This change from dextrorotation to laevorotation is called sugar inversion.
2. A nucleoside is formed from the combination of a nitrogenous heterocyclic base and a pentose sugar.
3. Enzymes act as biocatalysts and catalyze reactions in living organisms, such as the hydrolysis of sucrose by the enzyme invertase.
1. Sucrose undergoes hydrolysis to form an equimolar mixture of D-glucose and D-fructose, which has the opposite rotation of light compared to sucrose. This change from dextrorotation to laevorotation is called sugar inversion.
2. A nucleoside is formed from the combination of a nitrogenous heterocyclic base and a pentose sugar.
3. Enzymes act as biocatalysts and catalyze reactions in living organisms, such as the hydrolysis of sucrose by the enzyme invertase.
Original Description:
Original Title
28 imp QUESTIONS FINAL & LAST MINUTE REVISION QA
1. Sucrose undergoes hydrolysis to form an equimolar mixture of D-glucose and D-fructose, which has the opposite rotation of light compared to sucrose. This change from dextrorotation to laevorotation is called sugar inversion.
2. A nucleoside is formed from the combination of a nitrogenous heterocyclic base and a pentose sugar.
3. Enzymes act as biocatalysts and catalyze reactions in living organisms, such as the hydrolysis of sucrose by the enzyme invertase.
1. Sucrose undergoes hydrolysis to form an equimolar mixture of D-glucose and D-fructose, which has the opposite rotation of light compared to sucrose. This change from dextrorotation to laevorotation is called sugar inversion.
2. A nucleoside is formed from the combination of a nitrogenous heterocyclic base and a pentose sugar.
3. Enzymes act as biocatalysts and catalyze reactions in living organisms, such as the hydrolysis of sucrose by the enzyme invertase.
INVERT SUGAR- Sucrose is dextrorotatory each component in the solution is directly
(+66.5°) but after hydrolysis it gives an proportional to its mole fraction. Thus, for a equimolar mixture of D-(+)-glucose and D-(–)- solution of volatile liquidsA and B, PA µ xA and fructose, which is laevorotatory. This change of PB µ xB or PA = PA x Ao and PB = P x B B o specific rotation from dextrorotation to where PA and PB are partialvapour pressures, laevorotation is called inversion of sugar and xA and xB are mole fractions, PAo and PBo are the mixture obtained is called invert sugar. vapour pressure of purecomponents A and B 2. NUCLEOSIDE is a unit formed by the respectively. combination of nitrogen containing heterocyclic 11.DENATURATION OF PROTEINS: When a base and pentose sugar. protein in its native form is subjected to a 3. ENZYMES- Enzymes are termed as biocatalysts change, such as change in temperature or as they catalyse numerous reactions that occur change in pH, the hydrogen bonds are in the bodies of animals and plants to maintain disturbed. Due to this, globules unfold and helix life process e.g., invertase, pepsin, urease get uncoiled and protein loses its biological 4. AMINO ACIDS- Amino acids are the activity. This is called denaturation of protein compounds, whose molecule contains both the 12.The important characteristics of the carboxylic acid (–COOH) group and the amino TRANSITION ELEMENTS are: (i) All transition (–NH2) group of the various amino acids, the a- elements are metallic in nature. (ii) Transition amino acids are most important because they elements exhibit variable oxidation states. (iii) are the building blocks of proteins. Most of the transition elements form coloured 5. CARBOHYDRATES- Carbohydrates that yield a compounds. (iv) A number of transition large number of monosaccharide units on elements and their compounds show catalytic hydrolysis are called polysaccharides e.g., properties. starch, cellulose, gums etc. 13.NUCLEOTIDE- A nucleotide contains all the three basic components of nucleic acid i.e., a 6. SEMICARBAZIDE has two NH2 group But only pentose sugar, nitrogeneous base and a one is involved in Nucleophilic addition phosphoric acid. When nucleoside is linked to reaction- Semicarbazide has two –NH2 groups phosphoric acid at 5’ position of sugar moiety, but one of them (i.e., directly attached to C = O) we get a nucleotide is involved in resonance. Thus, electron density 14.TRANSITION METALS FORM A LARGE on this NH2 group decreases hence it does not NUMBER OF COMPLEXES due to following act as a nucleophile reasons:= Small size and high charge of the ions of transition metals.= Presence of vacant 7. The binary mixtures of liquids having same orbitals of appropriate energy which can accept composition in liquid and vapour phase and lone pairs of electrons donated by ligand boil at a constant temperature are called 15. THE E° VALUE FOR THE MN3+/MN2+ AZEOTROPES. couple is much more positive than that for 8. The excess of pressure which must be applied Cr3+/Cr2+ couple. ANS-:Mn2+has the to the solution side to prevent the passage of electronic configuration [Ar]3d5 which is half filled and hence very stable.Due to this the third solvent into it through a semipermeable ionisation energy of Mn is very high. Thus the membrane is called OSMOTIC PRESSURE much large thirdionisation energy of Mn (where 9. The properties of solutions which depend only the required change is d5 to d4) is mainly on the number of solute particles in the solution responsible for this. but independent of their nature are called 16.PEPTIDE LINKAGE- A peptide linkage is an COLLIGATIVE PROPERTIES. amide (—C|| O— NH —) linkage formed between —COOH group of onea-amino acid and 10.RAOULTS LAW- It states that for a solution of —NH2 group of other a-amino acid by loss of a volatile liquids, the partial vapour pressure of water molecule 17.ANILINE DOES NOT UNDERGO FRIEDAL CRAFT reaction - Aniline being a Lewis base 23. reacts with AlCl3 a Lewis acid and catalyst used in Friedel craftsreaction to form salt C6H5N +H2AlCl-3. Due to presence of a +ve charge on N-atom in the salt, thegroup N+H2AlCl3 acts as a strong deactivating group. It reduces the electron density in the benzene ring as a result of this aniline does not undergo Friedel-crafts reaction 18. WHY PRIMARY AMINES HAVE MORE BOILING POINT THAN TERTIARY AMINES- 24.WHY ALDEHYDES ARE REACTIVE THAN In primary amines, two hydrogen atoms are KETONES. This is due to steric and electronic present on N-atom and they undergo extensive reasons. Sterically, the presence of two intermolecular hydrogen bonding which results relatively large substituents in ketones hinders in association of molecules while in tertiary the approach of nucleophile to carbonyl carbon amines, no hydrogen atom is present on N- than in aldehydes having only one such atom. Hence there is no hydrogen bonding in substituent. Electronically two alkyl groups tertiary amines. As a result of this primary reduce the positivity of the carbonyl carbon amines have higher boiling point than tertiary more effectively in ketones than in aldehydes. amines. 25. Why are ethers insoluble in water? 19.KOHLRAUSCH LAW states that the limiting Ethers are insoluble in water because due to molar conductivity of an electrolyte can be the bigger size of the alkyl groups, the oxygen represented as the sum of the individual atom in ethers fails to form intermolecular H- contributions of cation and anion of the bonds with water. electrolyte. 26.Phenol is more acidic than methanol. 20.A reaction which is not truely of first order but In phenol, the phenoxide ion obtained after the under certain conditions becomes a reaction of removal of a proton is stabilised by resonance first order is called PSEUDO FIRST ORDER whereas there is no resonance in the alkoxide REACTION e.g. acid hydrolysis of ethyl acetate. ion of methanol. 21.HENRY`S LAW – It states that “the partial 27.Zn2+ salts are white while Cu2+ salts are pressure of the gas in vapour phase (p) is coloured. Why? directly proportional to the mole fraction of gas Ans. Cu2+ (3d 9 4s 0) has one unpaired electron in (x) in the solution”. Mathematically, p = KHx d-subshell which absorbs radiation in visible where KH is the Henry's law constant. The region resulting in d-d transition and hence Cu2+ solubility of a gas in liquid decreases with rise salts are coloured. Zn2+ (3d 10 4s 0) has in temperature as dissolution of a gas in a liquid completely filled d-orbitals. No radiation is is an exothermic process. absorbed for d-d transition and hence Zn2+ salts 22.WHY CARBOXYLIC ACID ARE MORE are colourless. STRONGER ACIDS THAN PHENOLS- Because 28.What is Tollens’ reagent? Write one the release of proton from carboxylic acid is usefulness of this reagent. much easier than from phenol as the conjugate Ans. Ammonical silver nitrate (AgNO3 + NH4OH) base carboxylate ion is much more resonance solution is known as Tollens’ reagent. It is used to stabilised than conjugate base phenoxide ion detect the presence of —CHO group in an organic compound.