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The factors, which increase the stability of carboxylate ion more than the carboxylic acids, increase the acidic strength of acid and the factors that decrease the stability of carboxylate ion decrease the acid strength In Benzoic acid the Phenyl group is directly attached to - COOH group. Gives overall electron releasing effect so unsubstituted C.Acids are stronger than aliphatic acids. The order of acidic strength is depending on Pka values as shown below Formic acid > Benzoic acid > Acetic acid. 
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I think you are talking about the acidic nature of carboxylic acids. The Methyl group is electron releasing in nature and causes +I effect which makes release of H+ difficult due to increase d electron density around c and finally O-H bond becomes stronger therefore its acidic character decreases
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BESIDES NCERT BOOK NO DOUBT MORRISON BYOD AND COREY BOOKS ARE GOOD. EVEN SOME BOOKS OF PRAGATI PARKASHAN ARE ALSO GOOD. INORGANIC CHEMISTRY : OP AGGARWAL IS BEST ORGANIC CHEMISTRY : O.P TANDON PHYSICAL CHEMISTRY : P.BAHADUR SHE IS ABSOLUTELY RIGHT BUT FOR BOARD PREPARATION NCERT IS THE BEST
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Free energy of a system is defined as the maximum amount of energy available to a system during a process that can be converted into useful work. In other words it is a measure of capacity of a system to do useful work. It is denoted by symbol G and is given by G = H-TS where H is the enthalpy of the system, S is its entropy and T is the absolute temperature. Now, H = E + PV so G = E + PV- TS
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| | Free energy of a system is defined as the maximum amount of energy available to a system during a process that can be converted into useful work. In other words it is a measure of capacity of a system to do useful work. It is denoted by symbol G and is given by |
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| G = H-TS where H is the enthalpy of the system, S is its entropy and T is the absolute temperature. |
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| Now, H = E + PV |
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| G = E + PV- TS |
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Answer of the question is 3 i.e. NaOI which is responsible for he formation of Iodoform2. q answer is 2 as h is replaed by Br and for stable product
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formaldehyde reacts with ammonia to form hexamethylene tetramine (CH2)6N4 also known as urotropine.
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The common name is Ethyl methyl ketone because alkyl groups are named alphabatically
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If you are taking about the calculation related to enrgy emitted during transition from one level to another The frequency of the emitted radiation is: v(nu) = E2-E1/h Since E2 and E1 have only definite values and are characteristic of energy levels of atoms, the values of 'n' will also be definite and characteristic of the atoms. Thus each transition will produce a light of definite wavelength, which is observed as a line in the spectrum. Corresponding frequency can be calculated(please write question very clearly)
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the formula is CH3CH2C(doublebond O)NH-C2H5 and Name will be N-Ethylpropanamide as mentioned by Krishan Gopal sing Sir
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Collision numberNumber of bimolecular collisions in 1 m3 per sec,Z11 (s-1m-3) = ½ N/V z11½ not to count collisions twice=1/?2 (N/V)2 ?d2?Vfor different molecules,Z12 = (NA/V) (NB/V) ? (r1 + r2)2 (8kT/? ?)½Collision Number is very large ~ 1034 for N2 at STP
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Total collision frequency for all molecules within a volume divided by that volume.Collision number now a days is called as collision density and is represented by Zaa
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Sodium is introduced into xylene. In which each methyl group takes one Na atom -..-00------------++++++++++++++++++Na is added to Xylenes to form Sodium alkyl . which are further used for alkylation. In other words xylenes can be further alkylated through addition of Na to xylenes
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Sodium is introduced into xylene. In which each methyl group takes one Na atom -..-00------------++++++++++++++++++Na is added to Xylenes to form Sodium alkyl . which are further used for alkylation. In other words xylenes can be further alkylated through addition of Na to xylenes
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Sodium is introduced into xylene. In which each methyl group takes one Na atom -..-00------------++++++++++++++++++Na is added to Xylenes to form Sodium alkyl . which are further used for alkylation. In other words xylenes can be further alkylated through addition of Na to xylenes
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question is not clear . what u actually want to know? You want to know natural sources of these elemens or their preparatione.g. Sodium is a regular part of our food supply. It is found naturally in meats, nuts, grains, fruits, vegetables, and dairy products in low amountsMagnesium is very abundant in nature, occurring in substantial amounts in many rock-forming minerals such as dolomite, magnesite, olivine, and serpentine. In addition, magnesium is also found in sea water, subterranean brines, and salt beds. It is the third most abundant structural metal in the Earth's crust, exceeded only by aluminum and iron.some natural sources of Fe are Almonds, Apricots,Beets (and greens),Chicken etc
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i dont know what happened to text i m writing answer againThe correct order is NCl3 < NF3 < NH3 this is due to the fact that bond strength depends upon the extent of overlapping between orbitals . In above compounds the overlapping is between 2p - and 3p orbitals , it is between 2p-2p in NF3 while it is between 2p-2s . The order of penetration towards nucleous is of order of s>p>d>f. So bond in NH3 is strongest where bond in NF3 is stronger than NCl3
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The correct order is of course NCl3p>d>f . as in case of ammonia s orbitals are involved so N-H bond is strongest among all NF3 is stronger than NCl3
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Electron affinity of Cl is more than that of F because fFhas exceptionally small size and the electrons present in F are compactly packed and further addition of an electron to F leads to repulsion as a result of which EA of F decreases than Cl
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While the two terms are often closely related, there is no exact parallel relationship between them. Basicity is a matter of equilibrium Based on Bronsted theory, water is a stronger base than chloride ion because the equilibrium favors the acceptance of a proton by water more than the acceptance of a proton by chloride ion. Nucleophilicity is a matter of kinetics (rate) Hydroxide ion is a better nucleophile than ammonia because hydroxide ion attacks carbon faster than ammonia. ? Basicity involves proton transfer ? Nucleophilicity involves attack rate at sp3 carbon
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