Wednesday, January 22, 2020

Ditte’s reaction-application-Deacon’s process in halogen chemistry


Ditte’s reaction in halogen chemistry


I2 O5 is a powerful oxidizing agent, which oxidize CO molecule in quantitative analysis to convert CO2 molecule along with molecular iodine .

Ditte’s reaction-application-Deacon’s process in halogen chemistry

Wednesday, January 8, 2020

Halogen elements-definition-properties-reactivity and uses.


Halogen  elements definition .

There are few electronegative as well as non metallic elements ,belongs to 17th group in the modern periodic table, are known as halogen elements . Halogen elements are fluorine, chlorine, bromine , iodine and astatine .   

Halogen  elements definition .

Among these , fluorine and chlorine are colourless  gaseous elements , bromine is brown color liquid and iodine is violet crystalline solid.  

The name ‘halogen’ means salt  producing .That is they produced  salt , when react with metals .The salts of first three occur in the sea water. 

Such as  sodium chloride ( NaCl ) , calcium fluoride ( CaF2 ), silver bromide ( AgBr ) and potassium iodide( KBr )  etc .

Halogen elements in periodic table.

According to modern periodic table , group 17th comprises of five elements , namely , fluorine, chlorine, bromine ,iodine and astatine which  do not occur free in the nature , are known as halogen elements .

In deed , fluorine, chlorine, bromine and iodine have closely related properties and are known  collectively as the halogen elements.

Halogen  elements properties

General electronic configuration of halogen elements are, ns2,np5 .That is the outer most shell of halogen atom contains seven electrons .

Hence halogen element have tendency to gain one more electron to complete their octet .

Consequently, halogen elements are non metal as well as strong electronegative . The electronegativity of halogen elements decrease as we move  from top to bottom along a group .

Halogen elements have  high affinity for electron, that is have a strong tendency to pick up electrons . For this reason , they exhibits strong  oxidizing power . 

They can oxidize metal as well as non metal . Although ,the oxidizing power decrease on moving down the group .

Halogen elements reactivity

All the halogen elements react with metals as well as with many non metals to form  halides. Fluorine is the most reactive among the halogen elements. 

The reactivity decreases when we move from top to bottom along a group .

For example, with sulfur fluorine forms  sulfur hexafluoride , chlorine forms sulfur tetrachloride , bromine forms sulfur dibromide whereas iodine does not react at all .

Another example of halogen elements reactivity are the interaction of halogens with water . 
Fluorine react with water fast with explosion  to form a mixture of ozone and oxygen . 


Halogen elements reactivity

Chlorine react with water in presence of sunlight  and bromine  react so much less readily, while iodine scarcely reacts with water .

The chemical reactions of chlorine and bromine elements with water under specific condition is shown below,


Halogen elements reactivity

All the halogen elements react with hydrocarbons but their reactivity decreases with increase in atomic number . 

Fluorine is most reactive towards hydrocarbons. It  decompose hydrocarbon and release free carbon atom . 

Halogen elements reactivity

Chlorine under goes substitution reaction with hydrocarbon. Bromine also shows substitution reaction with hydrocarbon but slowly . Iodine react with hydro carbon  under condition . 

Halogen elements Uses

There are a large number of use of halogens elements . Halogen elements used both in organic as well as in inorganic chemistry . 

In organic chemistry , halogen elements participate  in nucleophilic  and in addition reaction  to produced  a large number of halogen containing compounds . 

In inorganic  chemistry  there are a huge number of  halogenated compounds . Most important  compounds of halogen elements  are  halides , hydracids, oxyacids, pseudo halogen compounds inter halogen compounds  etc .

Halogen elements  is used in many organic reaction to produced  halogenated compounds . Iodine and bromine is used as laboratory reagents .

Halogen elements  is also used in every day our life . Such as chlorine is used to purify water .Chlorine is also a part of table salt  ( NaCl ) , which is most widely used  chemical compound.

Fluorine is used in different fluorides , which are added to water supplies to protect our tooth decay . 
Fluorine is also used to hardiest our enamel to prevent  tooth. HF is used in glass industry to prepare different type of glass .  

Chlorine compound that is bleaching powder is used to prevent the growth of bacteria . Chlorine is also used in paper making industry and plastics industry .

Bromine is in photography, to prepare medicine , in water purification and to prepare pesticides  and flame resistant plastics .

Iodine is used mainly  in iodometric and iodimetric titration and to prepare medicine ( tincture of iodine  ) .

 Which is the  strongest acid  among  HF, HCl, HBr and HI ?

The acidic strength of halogen acid depends on the degree of ionization in aqueous solution and also bond dissociation energy .

Generally, the degree of dissociation decreases with increasing bond dissociation energy .That is with increasing bond dissociation enthalpy, acidic strength decreases.

Since, the increasing order of bond dissociation energy of halogen acids are ,
              
Which is the  strongest acid  among  HF, HCl, HBr and HI ?
Therefore, the increasing acidic order of the above halogen acids are ,  
              
Which is the  strongest acid  among  HF, HCl, HBr and HI ?
Consequently, among the halogen acids (, HF ,  HCl  , HBr  and  HI  ), HI is the strongest  acid . 

Summary :

Halogen elements definition .
Halogen elements in periodic table .
Halogen elements properties .
Halogen elements reactivity .
Halogen elements uses .
Which is the strongest acid among HF, HCl , HBr and HI acid ? 


Wednesday, January 1, 2020

Schotten Baumann reaction-mechanism-application-Schotten Baumann reaction-phenol-aniline.


Schotten Baumann reaction .


The benzoylation of phenol is carried out in presence of aqueous NaOH  or pyridine solution . Because , Benzoyl chloride does not hydrolysed by base .

So, the benzoylation of phenol in presence of aqueous NaOH  solution gives phenyl acetate . This  reaction is known as Schotten Baumann reaction.



Monday, December 23, 2019

pyridine is more basic than aniline and acetic acid is more acidic than methanol .


Why is pyridine more basic than aniline?


The strength of basicity depends on the tendency to donate an electron to the electron deficient element, ion or group. 
In case of aniline, the lone pair of electrons on nitrogen atom takes part in the resonance with the pi electron of benzene ring.



Tuesday, December 17, 2019

Paracetamol-paracetamol used for-paracetamol side effects and paracetamol made of.


What is paracetamol?


Paracetamol or N-acetyl para aminophenol is an aromatic compound which is also known as acetaminophen

Paracetamol is an analgesic as well as antipyretic non narcotic drugs . It is used as a medicinal drugs to treat pain and fever.


Paracetamol-paracetamol used for-paracetamol side effects and  paracetamol made of.

Tuesday, December 10, 2019

friedel-crafts alkylation reaction- friedel crafts alkylation of benzene-anisole-phenol and chloro benzene


What is Friedel crafts alkylation reaction ?


When hydrogen atom of benzene ring be substituted by the alkyl group in presence of anhydrous aluminium chloride ( AlCl3 ) catalyst to produced alkyl benzene, then the reaction is is Friedel crafts alkylation reaction. 

It is an example of aromatic electrophilic substitution reaction.




Thursday, December 5, 2019

picric acid or 2,4,6-tri-nitro phenol more acidic than phenol .


Why is picric acid or 2,4,6-tri-nitro phenol more acidic than phenol?


2,4,6-tri nitro phenol is also known as picric acid .Picric acid is more stronger acid than phenol.
Because, picric acid or 2,4,6-tri nitro phenol contains three strong electron withdrawing – NO2 group.




 Due to – I effect and – R effect of – NO2 group, the density of electron on oxygen atom of O – H group very much decreases.

As a result, oxygen atom attract O – H bonded electron towards itself . Hence O – H  bond becomes more polar and more weak.



So, O – H  bond break very easily to release proton ( H+ ). Consequently, picric acid or 2,4,6-tri nitro phenol more acidic than phenol .


What is acidic order of  o-nitro phenol , m-nitro phenol and p-nitro phenol and why?


All the mono nitro phenols are more acidic than phenol. Because – NO2 group is a strong electron withdrawing group . 

Due to – I effect and – R effect, – NO2 group can attract electron from any position (ortho, meta or para). Hence, all the mono nitro phenols are more acidic than phenol.
The acidic order of mono nitro phenols with compare to phenol are,




Now, among the o-nitro phenol, m-nitro phenol and p-nitro phenol, only o-nitro phenol and p-nitro phenol can attract electron from - OH  group due to – R effect of –NO2 group.

 Because , due to presence of – NO2 group in ortho and para position , a conjugation takes place between the lone pair of oxygen atom of – OH group and – NO2 group through benzene nucleus . 

But, in case of m-nitro phenol, - NO2 group present in meta position . Hence in this case conjugation between lone pair of – OH group and – NO2 group does not occur.

So ,for meta isomer, the density of electron of –OH  group decrease due to – I effect only .

Hence the density of electron on oxygen atom is lowest for p-nitro phenol and highest for m-nitro phenol. As a result , oxygen atom attract O – H bonded electron towards itself .

Consequently, the – OH bond for p-isomer becomes more polar and more weak . But the – OH bond of m-nitro phenol becomes less polar. 

So p-nitro phenol gives proton ( H+ ) more easily than the other two isomers .Hence the acidic order of  o-nitro phenol , m-nitro phenol and p-nitro phenol are as follows,



Why o-nitro phenol and p-nitro phenol are more acidic than phenol?


O-nitro phenol and p-nitro phenol  are more acidic than phenol. Because – NO2 group is a strong electron withdrawing group . 

Due to – I effect  of– NO2 group, it can attract electron from any position ( ortho, meta or para ).

Besides this , for  – R effect of – NO2 group , a conjugation takes place between the lone pair of oxygen atom of – OH group and – NO2 group through pi bond of benzene nucleus . Hence, oxygen atom gets partially positive charge.



As a result , oxygen atom attract O – H bonded electron towards itself . Hence O – H  bond becomes more polar and more weak .

So, O – H  bond  of o-nitro phenol and p-nitro phenol break very easily to release proton ( H+ ) than phenol.
Consequently, o-nitro phenol and p-nitro phenol are more acidic than phenol.



Practice problem:



What is acidic order of  o-nitro phenol , m-nitro phenol and p-nitro phenol and why ?
Why is picric acid or 2,4,6-tri nitro phenol more acidic than phenol ?
Why o-nitro phenol and p-nitro phenol are more acidic than phenol ? 




Monday, December 2, 2019

Phenol is acidic or basic and Which is stronger acid phenol or cresol ?


Phenol is acidic or basic?


Phenol is an aromatic alcohol, which contain – OH group.The lone pair electron on oxygen atom of phenol participate in resonance with the pi electron of benzene 
nucleus.



Wednesday, November 27, 2019

Why boiling point of alcohol is higher than ether and alkane ?


Why boiling point of alcohol is higher than ether?


Oxygen is more electronegative than hydrogen. For this reason, O – H bond  of alcohol is polar one. 

As a result , alcohol molecules can form inter molecular hydrogen bond, through which alcohol molecules become associated and they are staying as gigantic molecule.

Hence, a large amount heat energy is required to break this large number of hydrogen bond .Consequently, the boiling point of alcohol molecule is very much higher.


Thursday, November 21, 2019

Why acetic acid is more acidic than phenol and Why phenol are more acidic than aliphatic alcohol ?


Why acetic acid is more acidic than phenol?


Both acetic acid and phenol are ionized in aqueous solution and give acetate and phenoxide anion respectively. Now ,the strength of acid depends on relative stability of their concerned anion ( conjugate base ).


Friday, November 15, 2019

Why ionic bond is non directional but covalent bond is directional?


Why ionic bond is non directional but covalent bond is directional?


Actually, there is no existence of ionic bond. Ionic bond is nothing but a force of electrostatic attraction between cationand anion, which is formed by the lose or gain of electrons.
Since there is no direction of electrostatic attraction force, so ionic bond or ionic valency has no specific direction.


Friday, November 8, 2019

Why CH3Cl is more active than C6H5Cl towards hydrolysis and What is Ulmann reaction ?


Why CH3Cl is more active than C6H5Cl towards hydrolysis?


In case of chloro benzene, the lone pair of chlorine atom takes part in resonance with the Ï€ electrons of benzene ring . As a result, the C –Cl bond in chloro benzene gets partially double bond character .