Chemistry
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New answer posted
3 months agoContributor-Level 10
As 3f-orbital does not exist as value of l cannot be equal to n, hence no electron can be accommodated.
New answer posted
3 months agoContributor-Level 10
ΔH_rxn = ΔH_f (N? O, g) + 3ΔH_f (CO? , g) – (2ΔH_f NO? , g) – 3ΔH_f (CO, g)
= 81 + 3* (– 393) – 2 * 34 – 3 (–110)
= 81 – 1179 – 68 + 330 = – 836 kJ
New answer posted
3 months agoContributor-Level 10
The number of chiral carbons in open-chain aldohexose (such as glucose) is four, therefore, the number of stereoisomers = 2? = 16.
New answer posted
3 months agoNew answer posted
3 months agoContributor-Level 10
One mole of water is converted to vapour at its boiling point which is 100°C and at 1 atm. For this process ΔG = 0. As phase transformation of water is an equilibrium process and at equilibrium, free energy change is always zero.
New answer posted
3 months agoContributor-Level 10
Sometimes, when maximum covalency is obtained, the halides become inert to water, thus SF? (or similarly CCl? ) is stable. This is because SF? is coordinately saturated and sterically hindered. Thus, SF? is inert to water, because of kinetic rather than thermodynamic factor.
A. PCl? + 4H? O → H? PO? + 5HCl
B. SiCl? + 4H? O → Si (OH)? + 4HCl
C. BCl? + 3H? O → B (OH)? + 3HCl
New answer posted
3 months agoContributor-Level 10
2CO (g) + O? (g) → 2CO? (g)
Δn_g = 2 – (2 + 1) = -1
ΔH = ΔE + Δn_g RT or ΔH = ΔE – 1RT
i.e. ΔH < E
New answer posted
3 months agoContributor-Level 10
All monosaccharides which differ in configuration at C? and C? gives the same osazone. Since, glucose and fructose differ from each other only in configuration at C? and C? therefore, they give the same osazone. All other options given in the questions do not satisfy this condition and hence, do not from the same osazone.
New answer posted
3 months agoContributor-Level 10
The second ionization energy of K is maximum, because the second electron is removed from fully filled 3p? subshell. The second ionization energies of group 2 elements decrease down the group.
Hence, second I.E. of Ca > second I.E. of Ba.
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