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TERM 2 OSWAAL BOOK 📚

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❌Stereoisomerism: This type of isomerism arises because of different spatial arrangement. ❌Geometrical isomerism: It arises in heteroleptic complexes due to different possible geometrical arrangements of ligands. ❌Optical isomerism: Optical isomers are those isomers which are non-superimposable mirror images. ❌❌Valence bond theory: According to this theory, the metal atom or ion under the influence of ligands can use its (n-1)d, ns, np or ns, np, nd orbitals for hybridisation to yield a set of equivalent orbitals of definite geometry such as octahedral, tetrahedral, and square planar. These hybridised orbitals are allowed to overlap with ligand orbitals that can donate electron pairs for bonding. Coordination Number and Type of hybridisation Shape of hybrid 4 Tetrahedral 4 Square planar 5 Trigonalbipyramidal 6 (nd orbitals are involved – outer orbital complex or high spin or spin free complex) Octahedral 6 d orbitals are involved –inner orbital or low spin or spin paired complex) ❌Magnetic properties of coordination compounds: 🔻A coordination compound is paramagnetic in nature if it has unpaired electrons and 🔻 diamagnetic if all the electrons in the coordination compound are paired. . ❌❌Crystal Field Theory: It assumes the ligands to be point charges and there is electrostatic force of attraction between ligands and metal atom or ion. It is theoretical assumption. Crystal field splitting in octahedral coordination complexes: Crystal field splitting in tetrahedral coordination complexes: For the same metal, the same ligands and metal-ligand distances, the difference in energy between eg and t2g level is ❌❌Metal carbonyls: Metal carbonyls are homoleptic complexes in which carbon monoxide (CO) acts as the ligand. 🌡️Example: The metal-carbon bond in metal carbonyls possess both s and p character. 🔻The M–C bond is formed by the donation of lone pair of electrons from the carbonyl carbon into a vacant orbital of the metal. 🔻The M–C bond is formed by the donation of a pair of electrons from a filled d orbital of metal into the vacant antibonding orbital of carbon monoxide. 🔻The metal to ligand bonding creates a synergic effect which strengthens the bond between CO and the metal.
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➥The Central Board of Secondary Education (CBSE) has released the complete datesheet for class 10 and 12 term 2 exams. The term 2 exams will be held from April 26. CBSE Website : https://www.cbse.gov.in/cbsenew/cbse.html ➥ Share & Support us :- @cbse_term_2_sample_papers_books
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Handwritten Physics All Important Derivations For Jee, Neet & Boards Study physics all chapters with these derivations in simple way. ━ Class XII Physics. ━ Final Revision. ━ For Board Exams & JEE. Shared with love by ❤️ @Term_2_oswaal_books
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⚡️ COMPLETE Chemical_Properties of Alkali Earth Metals: FROM NCERT ⚡️ 1. Reaction with water : Mg + H2O → MgO + H2 or, Mg + 2H2O → Mg (OH)2 + H2 Ca + 2H2O → Ca(OH)2 + H2 2. Formation of oxides and nitrides Be + O2 (air) +Δ→ 2BeO 3Be + N2 (air) +Δ → Be3N2 Mg + air + Δ → MgO + Ng3N2 3. Formation of Nitrides 3M + N2 + Δ → M3N2 Be3N2 + Δ → 3Be + N2 Ba3N2 + 6H2O + Δ → 3Ba (OH)2 + 2NH3 Ca3N2 + 6H2O + Δ → 3Ca (OH)2 + 2NH3 4. Reaction with hydrogen: M + H2 + Δ → MH2 Both BeH2 and MgH2 are covalent compounds having polymeric structures in which H – atoms between beryllium atoms are held together by three centre – two electron (3C - 2e) bonds as shown below: 5. Reaction with carbon – (Formation of carbides) When BeO is heated with carbon at 2175 – 2275 K a brick red coloured carbide of the formula Be2C is formed 2BeO +2C \xrightarrow[]{2175 - 2275 K}Be_2C +2CO It is a covalent compound and react water forming methane. Be2C + 4H2O → 2Be (OH)2 + CH4 6. Reaction with Ammonia: Like alkali metal, the alkaline earth metals dissolve in liquid ammonia to give deep blue black solution from which ammoniates [ M (NH3)6 ]2+ can be recovered. Anamolous Behaviour of Beryllium: Be is harder than other members of its group. Be is lighter than Mg. Its melting and boiling points are higher than those of Mg & other members. Be does not react with water while Mg reacts with boiling water. BeO is amphoteric while MgO is weakly basic. Be forms covalent compounds whereas other members form ionic compounds. Beryllium carbide reacts with water to give methane whereas carbides of other alkaline earth metals gives acetylene gas. Be2C + 4H2O → 2Be (OH)2 + CH4 Mg2C2 + 2H2O → Mg (OH)2 + C2H2 CaC2 + 2H2O → Ca (OH)2 + C2H2 Beryllium does not exhibit coordination number more than four as it has four orbitals in the valence shell. The other members of this group has coordination number Diagonal relationship of Be with Al: Unlike groups – 2 elements but like aluminium, beryllium forms covalent compounds. The hydroxides of Be, [Be(OH)2] and aluminium [Al(OH)3] are amphoteric in nature, whereas those of other elements of group – 2 are basic in nature. The oxides of both Be and Al i.e. BeO and Al2O3 are high melting insoluble solids. BeCl2 and AlCl3 have bridged chloride polymeric structure. The salts of beryllium as well as aluminium are extensively hydrolysed. Carbides of both the metal reacts with water liberating methane gas. Be2C + 4H2O → 2Be (OH)2 + CH4 AI4C3 + 12H2O → 4Al (OH)3 + 3CH4 The oxides and hydroxides of both Be and Al are amphoteric and dissolve in sodium hydroxide as well as in hydrochloric acid. BeO + 2HCI → BeCI2 + H2O BeO + 2NaOH → Na2BeO2 + H2O Al2O3 + 6HCI → 2AICI3 + H2O AI2O3 + 2NaOH → 2NaAIO2 + H2O Like Al, Be is not readily attacked by acids because of the presence of an oxide film. Calcium Carbonate (CaCO3): It occurs in nature as marble, limestone, chalk, coral, calcite, etc. It is prepared as a white powder, known as precipitated chalk, by dissolving marble or limestone in hydrochloric acid and removing iron and aluminium present by precipitating with NH3, and then adding ammonium carbonate to the solution; the precipitate is filtered, washed and dried. CaCl2 + (NH4)2CO3 →CaCO3 + 2NH4Cl It dissolves in water containing CO2, forming Ca(HCO3)2 but is precipitated from solution by boiling. CaCO3 + H2O + CO2 ↔️ Ca(HCO3)2
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