NEET 2021 | ऐल्कोहॉल, फीनौल एवं ईथर - L6 | Class 12 रसायन विज्ञान | Hindi Medium | Kamesh Sir | 4 PM

In iodometric titrations, an oxidizing agent such as KNnO_(4), K_(2)Cr_(2)O_(7),CuSO_(4),H_(2)O_(2) is allowed to react in neutral medium or in acidic medium with excess of potassium iodide to liberate free iodine Kl+ oxidizon agent to l_(2) Free iodine is titrated against stanard reducing agent usually with sodium thiosulphate i.e., K_(2)Cr_(2)O_(7)+6Kl+7H_(2)SO_(4)toCr_(2)(SO_(4))_(3)+4K_(2)SO_(4)+7H_(2)O+l_(2) 2CuSO_(4)+4Kl to Cu_(2)l_(2)+2K_(2)SO_(4)+l_(2) l_(2)+Na_(2)S_(2)O_(3)to 2Nal+Na_(2)S_(4)O_(6) In iodometric titrations, starch solution is used as an indicator. Starch solution gives blue or violet colour with free iodine. At the end point, blue or violet colour disappear when iodine is completely changed to iodide. A 1.1g sample of copper ore is dissovled and Cu^(2+) (aq.) is treated with Kl.l_(2) liberated required 12.12mL of 0.1M Na_(2)S_(2)O_(3) solution for titration. The % Cu in the ore in the ore is:

Two rigid adiabatic vessel A and B which initially ,contain two gases at different temperature are connected by pipe line with value of negligible volume .The vessel A contain 2 moles Ne gas (C_(p.m)=(5)/(2)R) at 300 K, vessel B contain 3 moles of SO_(2) gas (C_(p.m)=4 R) at 400 K . The volume of the A and B vessel is 4 and 6 litre repectively . The final total pressue (in atm ) when valve is opened and 12 kcal heat supplied throught it to vessels . [Use : R =2 cal //"mole" K "and" R=0.08 L . atm//"mole" K as per desire ]

Class 12 Physics (Hindi) | Chapter 4 गतिमान आवेश एवं चुम्बकत्व | Important Questions and Quick Revision

Early crystallographers had trouble solving the structures of inorganic solids using X-ray diffraction because some of the mathematical tools for analyzing the data had not yet been developed. Once a trial structure was proposed, it was relatively easy to calculate the diffraction pattern, but it was difficult to go the other way (from the diffraction pattern to the structure) if nothing was known a priori about the arrangement of atoms in the unit cell. It was important to develop some guidelines for guessing the coordination numbers and bonding geometries of atoms in crystals. The first such rules were proposed by Linus Pauling, who considered how one might pack together oppositely charged spheres of different radii. Pauling proposed from geometric considerations that the quality of the "fit" depended on the radius ratio of the anion and the cation. If the anion is considered as the packing atom in the crystal, then the smaller catin fills interstitial sites ("holes"). Cations will find arrangements in which they can contact the largest number of anions. If the cation can touch all of its nearest neighbour anions then the fit is good. If the cation is too small for a given site, that coordination number will be unstable and it will prefer a lower coordination structure. The table below gives the ranges of cation/anion radius ratios that give the best fit for a given coordination geometry. {:("Coordiantion number","Geometry",rho =(r_("cation"))/(r_("amion"))),(2,"linear",0-0.155),(3,"triangular",0.155 - 0.225),(4,"tetrahedral",0.225 - 0.414),(4,"square planar",0.414 - 0.732),(6,"octahedral",0.414 - 0.732),(8,"cubic",0.732 - 1.0),(12,"cuboctahedral",1.0):} (Source : Ionic Radii and Radius Ratios. (2021, June 8). Retrieved June 29, 2021, from https://chem.ibretexts.org/@go/page/183346) The radius of Ag^(+) ion is 126 pm and of I^(-) ion is 216 pm. The coordination number of Ag^(+) ion is :

Early crystallographers had trouble solving the structures of inorganic solids using X-ray diffraction because some of the mathematical tools for analyzing the data had not yet been developed. Once a trial structure was proposed, it was relatively easy to calculate the diffraction pattern, but it was difficult to go the other way (from the diffraction pattern to the structure) if nothing was known a priori about the arrangement of atoms in the unit cell. It was important to develop some guidelines for guessing the coordination numbers and bonding geometries of atoms in crystals. The first such rules were proposed by Linus Pauling, who considered how one might pack together oppositely charged spheres of different radii. Pauling proposed from geometric considerations that the quality of the "fit" depended on the radius ratio of the anion and the cation. If the anion is considered as the packing atom in the crystal, then the smaller catin fills interstitial sites ("holes"). Cations will find arrangements in which they can contact the largest number of anions. If the cation can touch all of its nearest neighbour anions then the fit is good. If the cation is too small for a given site, that coordination number will be unstable and it will prefer a lower coordination structure. The table below gives the ranges of cation/anion radius ratios that give the best fit for a given coordination geometry. {:("Coordiantion number","Geometry",rho =(r_("cation"))/(r_("amion"))),(2,"linear",0-0.155),(3,"triangular",0.155 - 0.225),(4,"tetrahedral",0.225 - 0.414),(4,"square planar",0.414 - 0.732),(6,"octahedral",0.414 - 0.732),(8,"cubic",0.732 - 1.0),(12,"cuboctahedral",1.0):} (Source : Ionic Radii and Radius Ratios. (2021, June 8). Retrieved June 29, 2021, from https://chem.ibretexts.org/@go/page/183346) A solid AB has square planar structure. If the radius of cation A^(+) is 120 pm, calculate the maximum possible value of anion B^(-) .