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Showing posts with label ACIDS AND BASES. Show all posts
Showing posts with label ACIDS AND BASES. Show all posts

Tuesday, May 4, 2021

How to pridict cyclic structure given compound/oxy-acid:

 If  in given compounds number of substituents are integral multiple of central atoms (except P4O6,P4O10,P4S3,P4S10,(CH2)6N4,B4Cl4) the compounds  will be cyclic structure. And number of central atoms must be three (3) or more than three. 

Meta phosphoric acids and their salts always exist in dimeric, trimeric, tetrameric or in polymeric linear as well as cyclic form, not in monomeric form due to the presence of weak (2p-3d- pi bond) bond the sodium salts of trimer and hexamer is very famous salts.

How to find oxy-linkage present in a given oxy-acid:


 Related Questions:

What are "pyro" oxy acids?

What are "Ortho" or "Meta" oxyacids?

How to find oxy-linkage present in a given oxy-acid:

 If calculated/avarage oxidation state of central atoms in an oxy acid/oxyanion /oxide having two or more central atomis found to be one of the its common oxidation state then oxy-linkage will be present however this rule is not applicable for hyponitrous acid(H2N2O2), thiosulphuric acid(H2S2O3) and pyrosulphuric acid (H2S2O5).

For example H6P4O13  has calculated/avarage oxidation state of p=+5 and one of common oxidation state of p is +3 and +5 it means calculated oxidation state match with common oxidation state so there is oxy-linkage(P-O-P) present.

 Related Questions:

What are "pyro" oxy acids?

What are "Ortho" or "Meta" oxyacids?

Prefix “Hypo-acids”, and “Per-acids”:

 The prefix “Hypo” use for those oxy acid having lower oxidation state than either “us” or “ic” oxy acid for example Hypophosphorous acid (H3PO2), Hypophosphoric acid (H4P2O6)  and hyposulphurous acid (H2S2O4). For exitence of hypo acid  for an oxy acid, it must be a parent oxy acid contains at least two hydrogen atoms except nitrous acid (HNO2).

Example; Which of the following parent acid does/do not has correspong “Hypo” oxy acid?

(A) HNO3 (B) H3PO4 (C) H2SO4 (4) HClO4

Answer Key : A and D

The prefix “per” used to an oxy acid  which is obtained by adding one oxygen atom to the a respective “ic oxy acids” for example sulphuric acid (H2SO4) and its per sulphuric acid/caro’s acid is (H2SO5) which is contains one (-O-O-) peroxy linkage. And also hydrochloric acid (HClO4) and Perhydrochloric acid (HClO5).

Per-acid having two central atoms is formed by adding one oxygen atom to its pyro-ic-acid. For pyrosulphuric acid (H2S2O7) and pyrophosphoric acid (H4P2O7) and their per-oxy-acids are perdisulphuric acid/marshal’s acid (H2S2O8) and perdiphosphoric acid (H4P2O8) repectivily.

Conclusion: If –OH group attach to that central atom having lone pair and vacant orbitals and tendency to expand its orbitals then there is possibility of tautomerised. If size of central atom is should be small then there will be no tautomerism, so in case of Antomony,Arsenic while drawing structure of oxy acids all the hydrogen atoms are converted into –OH groups and they are symmetrical bonded to all central atoms. How ever this rule is not applicable for those oxy acidsof phosphorous in which oxidation state of phosphorous is +1 or +3.

Basicity of an oxy acid is equal to number of –OH groups presents in it exceptin oxy acid of boron. Oxy acid of boron does not furnish H+ rather it act as Lewis acid.

Related Questions: 

Suffix – “ic-acids” , ‘us-acids” :

The preffix “us” use for the those oxy acids which have one of the lower common oxidatation state while preffix “ic” use for those oxy acid have one of the higher oxidation state for example the common positive oxidation state of  nitrogen is its oxy acid HNO2 is (+3) and HNO3 is (+5) so  HNO2 named as nitrous acid while HNO3 is named as nitric acid. And  other example of Sulphurous acid H2SO3(+4) and sulphuric acid H2SO4(+6).

 Related Questions:

What are "pyro" oxy acids?
Why SF6 behave inert towards hydrolysis?
What are the SESQUI OXIDES ? give the examples.
Arrange in increasing order of extent of hydrolysis [ CCI4, MgCI2, AICI3, PCl5, SiCI4].
Although Sulphur contain vacant d-orbital but SF6 does not under go hydrolysis. Why ?
CCl4 can not be hydrolysed but SiCl4 can be. Why?
Silianol (SiH3OH) is more acidic than methanol (CH3OH) why?

Pyro-oxy acids:

The term "Pyro" use for those oxy acid which are formed by removal of one water molecule from two molecules of same oxy acid and resulting product is also an oxy acid then the product acid is named with prefix "Pyro"

For Examples:

H3BO3 (), H2CO3 (), H4SiO4 (), HNO3 (×), HPO3 (), HPO4 (), H2SO4 (), HCl4 (×)

(×) "Pyro" form not possible.

() "Pyro" form possible.

(1) In general those oxy acids are formed “pyro” acid which contains atleast two hydrogen atoms.

(2) In general all the “pyro” oxy acids contain oxy-linkage except "pyro sulphurous acid"

 Related Questions:

What are "pyro" oxy acids?

What are "Ortho" or "Meta" oxyacids?






Solvolysis in Liquid HF:

 


Related Questions: 

What is Use of Boric Acid?

What is use of Orthoboric acids?

What is basicity of "Boric acid" ?

Why Boric acid exist in solid state ?

What is structure of solid Ortho Boric acid ?

What is effect of heat on Borax?


Solvolysis in Liquid SO3:

(A) Solvolytic reaction takes place in liquid solvents like SO2 and NH3

(B) Acid –Base reaction in liquid (SO3):


 Related Questions:

What are "pyro" oxy acids?

What are "Ortho" or "Meta" oxyacids?




Auto ionization of anhydrous Sulphuric acid:

 Anhydrous  sulphuric acid is an  acidic Solvent the main auto ionization is

(1) The Mobility of H3SO4+ and HSO4-  are comparable to H3O+ and  OH- and most of acid accept H+ from H2SO4  and thus behave as base. For example H2PO4 and HNO.

(2) HClO4 and HFSO3 are very strong acid in water but very poor weak acid in sulphuric acid. 


Related Questions: 

What is Use of Boric Acid?

What is use of Orthoboric acids?

What is basicity of "Boric acid" ?

Why Boric acid exist in solid state ?

What is structure of solid Ortho Boric acid ?

What is effect of heat on Borax?

What is the structure of trimetaboric acid and trimetaborate ion?

What is the Sodium per borate ,give the structure and its uses?

Why aqueous solution of borax reacts with two moles of acids ?

What is the molecular formula of Borax ?

Why Boric acid become strong acid in the presence of cis 1,2-diol or 1,3-diol ?

Why Borazine is more reactive than benzene towards Electrophic Aromatic substitution reactions ?

Why Borazine (B3N3H6) is also known as inorganic benzene ?.


 

Solvolysis in liquid NH3 (Ammonolysis):

 

 Related Questions: 

Why aqueous solution of AlCl3 is acidic in nature ?

What happen when aq AlCl3 react with Acid or Base?

Although anhydrous aluminium chloride is covalent but its aqueous solution is ionic in nature. Why?

Why BF3 do not exist as dimer?. Explain.

Why B-F bond length in BF3 is shorter (130 pm) than B-F bond Iength in BF4- (143 pm)?. Explain.

B-F bond length in BF3 is shorter than B-F bond length in (BF4)- why?

When B2H6 is allowed to react with following Lewis bases, then how may given Lewis base form adduct through symmetrical Cleavage of B2H6.

What is product of reaction between diborane (B2H6) and ammmonia (NH3)?

Why methylation of Diborane (B2H6) replace four hydrogen only ?


Hydrolysis reactions:


Related Questions:

What are the SESQUI OXIDES ? give the examples.

Solvolysis in liquid N2O4:

 

Related Questions:

What are the SESQUI OXIDES ? give the examples.

Thursday, January 14, 2021

What are the oxy-acids?

Oxyacids:

The acids contains oxygen and must have one -OH group directly attach with central atom and also oxidation state of central atom is (+) positive. Most of covalent (acidic) oxide react with water to form oxy-acid that yield hydronium (H3O+)ions in solution. Mostly non metal of P-block formed oxy-acids except some metals.

Strength of Oxy acid:

The strenght of oxy acid define by degree of dissociation (pka) in water or ability to furnise H+ ions in water.

In general the relative strength of oxy acid can pridicted on the basis of electronegativity and oxidation state of central non metal atom.

(1) For example perchloric (HClO4) is stronger acid than sulphuric acid (H2SO4), which should be a stronger acid than phosphoric acid (H3PO4) because the electronegativity of the central atom increses as (Cl>S>P).

Acidic srength of acid as :  (HClO4)>(H2SO4)>(H3PO4)

(2) For given non metal acid the strength of oxy acid increases as the oxidation state of central atom increases for example sulphuric acid (OS=+6) (H2SO4) is more acidic then sulphurous acid (OS=+4)(H2SO3). Similarly nitric acis (HNO3)(OS=+5) is more acidic than Nitrous acid(HNO2)(OS=+3).

Acidic srength of acid as : 

(1) (H2SO4)>(H2SO3)

(2) (HNO3)> (HNO2)

(3) (HClO4)>(HClO3)>(HClO2)>(HClO)

Special Note: Oxy acid of phosphorous do not follow the concept of oxidation state. Because acidic strength of  phosphorous acid depends upon degree of dissociation (Ka or Pka value): the order  acidic nature follow as H3PO2 > H2PO3 > H3PO4

Levelling effect and relative strength of acids:

When strong acids like HClO4, HCl, HBr, HI, HNO3 etc are dissolved in water they are equally ionised (100%) it means they are equally strong in water this is called levelling effect of water.
Similarly for strong bases also , NaOH, KOH  Ca(OH)2 etc are in water behave the same. hence relative strength of strong acids or base can not be compare in water .
(1) Water does no show levelling effect for weak acids or base because they are ionised upto different extent in water.
(2) All the acids are stronger than H3O+ ion, consider as strong acids and weak than H3O+ ion are consider as weak acids.
(3) All the bases stronger than OH- are consider as strong base and weaker than OH-, then they are consider  as weak base.

Definition: If more than one acids or bases are showing same acidic or basic strength in same solvent it is called labelling effect and the solvent is called labelling solvent for example:

(1) HClO4 and HI equally dessociation in aqueous medium (99.99%)  it means they have equal strength.

(2) HCl, HNO3  and H2SO4 are equally strong in water because their strength are “levelled” to solvent species H3O+. only by putting them into a more acidic solvent do they weak acids. With determinate Pka values which differetiate their strengths. Thus in glacial ethanoic acid (acetic acid ) as solvent, the order of  acidic strength is as: H2SO4 > HCl > HNO3 .
(3) Similarly HF and HCl are equally dessociation in NaOH (100 %).
If their strength differ in same solvent ,it is called
differential effect and the solvent is called differential solvent.

(4) For example HClO4 dessociate 99.99 % in acetic acid while HI dissociate 99.8% in acetic acid, it means acidic strength of HClO4 is more than HI in acetic acid.

(5) Many of inorganic oxoacid are strong acid (with more negative Pka value) inaqueous solution. But, as we have seen, use of solvent with a lower proton affinity than water like acetic acid, makes it possible to differentiate between the strength of these acids and measure Pka value.

H2CO3 < H3PO4 < H2SO4 < HClO4 (Increasing acidic sterngth) these acidic strength can  also explain if the folmulae of the these oxy acids are written as base or OH formate or like that OC(OH)2 < OP(OH)3< O2S(OH)2< O3Cl(OH) then it is clear that the acidic strength incrases as the number of oxygen atoms not involve in O-H bonding increases.
The reason behind
levelling and diffential  effect is ability of solvent to donate or accept protons .
For acids, acidic solvents are differential and basic solvent are levelling.

 Related Questions:

What are "pyro" oxy acids?

What are "Ortho" or "Meta" oxyacids?