Monday, May 10, 2021

Riemer Tiemann reaction

              Reimer Tiemann reaction 


Table contents:

History

About reaction

Mechanism

Comparasion

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History-

Riemer Tiemanm reaction is discovered by karl reimer ( 1845-1883 ) and Ferdinand Tiemann ( 1856-1883 ).


About reaction-

Riemer Tiemann reaction is substitution reaction . This reaction used for the orthoformylation of phenols.

When phenol is treated with chloroform in the presence of sodium hydroxide,an aldehyde group introduced at the ortho position. The reaction is called reimer tiemann reaction.



Mechanism-

1.Deprotonation of chloroform in the presence of strong base ( sodium hydroxide) 

And now chloroform carbanion forms.

2.chloroform carbanion undergoes alpha elimination and now dichlorocarbene formed as product.

3.sodium hydroxide deprotonates the phenol reagent.

4.Negative charged is delocalized into the benzene ring.

5. Nucleophile attack on the dochlorocarbene, forming an intermediate chloromethyl substituted phenol.

6.Finally we achieve hydroxy benzaldehyde.


ЁЯСЙЁЯСЙ Phenol is converted into hydroxy benzaldehyde via chloroform.Carbene is highly electron deficient due to electron withdrawing nature of its two chlorine group.


Comaparasion to other methods-

Directly we can formylation of aromatic compounds bh various method such as the gattarmann reaction, gattarman koch reaction, and Duff reaction, haak reaction but the safety of reaction the Reimer Tiemann reaction is the most advantage routine in chemical synthesis.


тЮбя╕П Riemer Tiemann reaction can be useful to yield phenolic acids by carbon tetrachloride product will be salicylic acid rather than the salycyladehyde.




Saturday, May 8, 2021

IITJAM 2022 exam pattern and prepration tips

                              IITJAM


1.What is IITJAM ?

 JAM ( joint admission test ) is an entrance test for masters which is conducted by IIT's or IISC banglore.

If you are interested in research then IITJAM exam is perfect for you . JAM offers you 2000+seats in IITs NITs and IISC for MSC + MSC PHD etc.


2. Subjects for IITJAM ?

There are total 7 subjects ( Physics, chemistry, mathematics, geology, biotechnology,mathematical statics economics ) 

*IISC banglore had added a new subject economics in 2021.


3. Qualification for IITJAM ?

ЁЯОУNationalty - indian/overseas

ЁЯОУbechlors In science

ЁЯОУIn qualifying degree aggregate at least 55% or 5.5 in out 10 for gen/obc.

 50% or 5.0 in out of 10 for sc/st.

Most of institute required maths in the 10+2 level.


4.What is JAM exam pattern ?

It's important to know about exam pattern .Exam paper is divided in three sections, every part/section have different pattern of questions as follows;

ЁЯСЙ Multiple choice question (MCQ) 

   In four options we can choose only one answer.

ЁЯСЙ Multiple Select answer (MSQ)

   In four options we can choose more than one answer.

ЁЯСЙ Numerical answer type (NAT)

  These questions do not have any option.NAT can be any numerical value or decimal or integer value тАж


5.About exam schedule ?

Time. 3 hours

Mode. online

Exam frequency.  once  a year



IITJAM exam preparation tips:

тЮбя╕ПSolve the previous year question.

тЮбя╕П Practice of mock test.

тЮбя╕ПRefer important book's question.


тЮбя╕ПMake short notes.

тЮбя╕ПAnd must study 5-6 hours daily.



friedal craft reaction and mechanism


                  Friedal-craft reaction


Table contents:

History

About reaction

Mechanism

Advantage

Limitations

Example


History-

Friedal craft reaction is discovered by charles friedal ( french scientist ) and james crafts ( American chemist ) in 1877.


About reaction-

Frieda crafts reaction is an electrophilic aromatic substitution reaction including organic coupling reaction. Friedal craft reaction are two type:

-Frieda craft alkylation

-Frieda craft acylation

This reaction involves the replacement of hydrogen atom via an electrophile.

The reactant for this reaction is aluminum trichloride, it is acts as Lewis acid and it is used in generating an electrophile in the process.


ЁЯСЙ Friedal craft alkylation:

This reaction helps in generating alkyl banene via alkyl halide as reactants. The catalyst is aluminum trichloride. Friedal craft alkylation indicate the replacement of an aromatic proton with an alkyl group.

In this reaction carbocation will be generate as intermediate.


Mechanism:

1.The formation of carbocation using Lewis acid aluminium trichloride.

2.Carbocation attack on the aromatic ring.

3.deprotonation of the intermediate will be. And the proton goes to on hydrochloric acid, regenerating aluminium trichloride catalyst.



ЁЯСЙ Frieda craft acylation:

It is the acylation of the aromatic rings, in this reaction involves the addition of the acyl group to aromatic ring. In this reaction reactant is the acid chloride and the catalyst is aluminium trichloride.The reaction is between benzene and acyl chloride under the condition. Lewis acid generate a highly electrophilic acylium kon which is stabilized by resonance.



Mechanism:

Step 1. Forming of acylium ion.



Step 2. Acylium ion attack on the aromatic ring and the aromaticity of the ring.


Step 3. Intermediate complex is deprotonated.


Step 4. Ketone product is formed adding water.


Advantage:

Acylation and alkylation are the advantage of friedal craft reaction.


Limitations:

Friedal craft reaction's limitations are carbocatiom rearrangement and polyalkyaltion . Acylation reaction yields only ketones.  Aryl amines can not be formed in this reaction.


Example

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Wednesday, May 5, 2021

Sandmayer Reactions , mechamism , example , uses

                       Sandmayer reaction

-Table of contents

: History

: About reaction

: Mechanism

:Uses

: Frenquely asked questions

: Example

-History

Traugott sandmayer ( swiss scientist ) discovered sandmayer  reaction in 1884 

during experiment to synthesize polyacetylene from benzene diazonium chloride and cuprous acetylide.

The product was phenylchloride of the Mr.sandmayer's reaction.


Reactant -aromatic amine

product  - arylhalide

Intermediate- nitrosamine

Reaction type - Radical nucleophilic aromatic substitution


Sandmayer reaction is the substitution reaction of an aromatic amino group.This substitution will be via nucleophile, proceed under Cooper catalysis.

Sanmayer reaction is used in the production of aryl halide.

It is used to transformation on benzene ( hydroxylation,trifluoromethylation,cynation, and halogenation )


-Mechanism

1.Formation of nitrosonium ion

2.Benzenediazonium formation 


Formation of nitrosonium ion

-at first we take sodium nitrate and acid 

-then water is removed in reaction

-nitrosonium ion reacts as an electrophile and it is reacted with an heterocyclic amine to form diazonium salt.



Benzenediazonium ion formation

-amine and nitrosonium ions will make benzenediazonium ion.


Uses:

-one important use is formation of an aryl halide

-It is used as synthesis of chloroform,iodoform etc.


Frenquely asked questions:

1.what type of sandmayer reaction?

 Ans: substitution reaction


2. Difference between sandmayer and gattarman reaction !

 Ans: In sandmayer reaction reactant is CuCl in HCl but in gattarman reaction reactant is CuCl or CuBr in chlorobenzene.


3.What is importance of sandmayer reaction?

 Ans: sandmayer reaction is important for transformation of benzene.


4.what is use of CuCl in sandmayer reaction ?

 Ans: It is react like nucleophile.


Example:
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Tuesday, May 4, 2021

Coordination compounds

                   Coordination compound


Those compounds that have a central metal which is an atom or ion form a coordinate bond with another neutral or ion, are called coordination-compounds.



Table of contents: 


1.Important terms


2.what is ligands and their types


3.oxidation number 


4.coordination polyhedron


5.homoleptic and heteroleptic complex



1. Key words

 

ЁЯСЙ Doublesalts- They are also called lattice compounds, these compounds are stable in solid state.


 Example - mohar salt




 ЁЯСЙ Complex compounds  - They are stable in both solid and solution states.




 ЁЯСЙ Central Ion - The cation or neutral metal atom that binds two or more anions or molecules is called a central ion.



 The central ion is the receiver.


ЁЯСЙ Coordinate Circles and Ionic Circles - The central metal and ligands are written in square brackets, this square bracket is called coordinate circle.


 The part outside the square bracket is called the ionic circle.



:What is a ligand and its types -


 Anions with single electron pairs are called ligands.


 The atom giving electron in the ligand is called donor atom.

  

1.monodentate ligand - those ligands that have only one donor.



 2. Bidentate ligands - containing two donor atoms.



 3. Tridentate ligand - containing three donor atoms.



 4. Quad ligand- containing four donor atoms.



 5.ambidentate ligand - monoental ligandthat has more than one donor atom.

Example- Nitro



 6. Chalate ligand- Polygonal ligand binds to two or more donor atoms with a central metal and forms a ring.

Example-ethylene diamine and oxalato



Oxidation number


 Rule-


 1. In neutral complex the sum of the charges of the central metal atom and the ligand is zero.


 2. Oxidation number is the sum of charges of metal atoms and ligands.



 Examples-


:Homoleptic and heteroleptic complex -


 In which donor atoms are attached to the same type of donor group, it is called homoleptic.



 In which donor atoms are attached to more than one type of donor groups, it is called heteroleptic complex.



:Coordination polyhedron - The arrangement of the ligands attached to the central metal is called the coordination polyhedron.








                    рдЙрдкрд╕рд╣рд╕рдпреЛрдВрдЬрдХ рдпреМрдЧрд┐рдХ


рд╡реЗ рдпреЛрдЧрд┐рдХ рдЬрд┐рдирдореЗ рдХреЗрдВрджреНрд░реАрдп рдзрд╛рддреБ рдЬреЛ рдкрд░рдорд╛рдгреБ рдпрд╛ рдЖрдпрди рд╣реЛрддрд╛ рд╣реИ рдЕрдиреНрдп рдЙрджрд╛рд╕реАрди рдпрд╛ рдЖрдпрди рдХреЗ рд╕рд╛рде рдЙрдкрд╕рд╣рд╕рдпреЛрдВрдЬрдХ рдмрдиреНрдз рдмрдирд╛рддрд╛ рд╣реИ, рдЙрдкрд╕рд╣рд╕рдпреЛрдВрдЬрдХ рдпреЛрдЧрд┐рдХ рдХрд╣рд▓рд╛рддреЗ рд╣реИред 


рд╡рд┐рд╖рдпрд╕реВрдЪреА:


 1. рдкреНрд░рдореБрдЦ рд╢рдмреНрдж


 2. рд▓реАрдЧреЗрдВрдб рдХреНрдпрд╛ рд╣реИ рдФрд░ рдЙрдирдХреЗ рдкреНрд░рдХрд╛рд░ 


 3. рдСрдХреНрд╕реАрдХрд░рдг рд╕рдВрдЦреНрдпрд╛


 4. рд╕рдордиреНрд╡рдп рдлрд▓рдХ


 5.рд╣реЛрдореЛрд▓реЗрдкреНрдЯрд┐рдХрдФрд░ рд╣реЗрдЯреНрд░реЛрд▓реЗрдкреНрдЯрд┐рдХ рдХреЙрдореНрдкреНрд▓реЗрдХреНрд╕ 



1.рдкреНрд░рдореБрдЦ рд╢рдмреНрдж


ЁЯСЙ  рджреНрд╡рд┐рдХ рд▓рд╡рдг- рдЗрдиреНрд╣реЗрдВ рдЬрд╛рд▓рдХ рдпреМрдЧрд┐рдХ рднреА рдХрд╣рддреЗ рд╣реИ рдпреЗ рдпреМрдЧрд┐рдХ рдареЛрд╕ рдЕрд╡рд╕реНрдерд╛ рдореЗ рд╕реНрдерд╛рдпреА рд╣реЛрддреЗ рд╣реИ 

рдЙрджрд╛рд╣рд░рдг- рдореЛрд╣рд░ рд╕рд╛рд▓реНрдЯ


ЁЯСЙрд╕рдВрдХреБрд▓ рдпреЛрдЧрд┐рдХ- рдпреЗ рдареЛрд╕ рдУрд░ рд╡рд┐рд▓рдпрди рдЕрд╡рд╕реНрдерд╛ рджреЛрдиреЛрдВ рдореЗрдВ рд╕реНрдерд╛рдпреА рд╣реЛрддреЗ рд╣реИред

рдЙрджрд╛рд╣рд░рдг- 



ЁЯСЙ рдХреЗрдВрджреНрд░реАрдп рдЖрдпрди - рдзрдирд╛рдпрди рдпрд╛ рдЙрджрд╛рд╕реАрди рдзрд╛рддреБ рдкрд░рдорд╛рдгреБ рдЬрд┐рд╕рд╕реЗ рджреЛ рдпрд╛ рдЙрд╕рд╕реЗ рдЕрдзрд┐рдХ рдЛрдгрд╛рдпрди рдпрд╛ рдЕрдгреБ рдмрдВрдзрд┐рдд рд╣реЛ рдХреЗрдВрджреНрд░реАрдп рдЖрдпрди рдХрд╣рд▓рд╛рддрд╛ рд╣реИред

рдХреЗрдВрджреНрд░реАрдп рдЖрдпрди рдЧреНрд░рд╛рд╣реА рд╣реЛрддрд╛ рд╣реИ 


ЁЯСЙ рд╕рдордиреНрд╡рдп рдордВрдбрд▓ рдФрд░ рдЖрдпрдирд┐рдХ рдордВрдбрд▓ -  рдХреЗрдВрджреНрд░реАрдп рдзрд╛рддреБ рдУрд░ рд▓рд┐рдЧреЗрдВрдб рдХреЛ рд╡рд░реНрдЧрд╛рдХрд╛рд░ рдХреЛрд╖реНрдардХ рдореЗрдВ рд▓рд┐рдЦрддреЗ рд╣реИ рдЗрд╕ рд╡рд░реНрдЧрд╛рдХрд╛рд░ рдХреЛрд╖реНрдардХ рдХреЛ рд╕рдордиреНрд╡рдп рдордВрдбрд▓ рдХрд╣рддреЗ рд╣реИред 

рд╡рд░реНрдЧрд╛рдХрд╛рд░ рдХреЛрд╖реНрдардХ рдХреЗ рдмрд╛рд╣рд░ рдХрд╛ рднрд╛рдЧ рдЖрдпрдирд┐рдХ рдордВрдбрд▓ рдХрд╣рд▓рд╛рддрд╛ рд╣реИред 


: рд▓рд┐рдЧреЗрдВрдб рдХреНрдпрд╛ рд╣реЛрддрд╛ рд╣реИ рдФрд░ рдЙрд╕рдХреЗ рдкреНрд░рдХрд╛рд░-

 рдПрдХрд╛рдВрдХреА рдЗрд▓реЗрдХреНрдЯреНрд░рд╛рди рдпреБрдЧреНрдо рд╡рд╛рд▓реЗ рдЛрдгрд╛рдпрди, рд▓рд┐рдЧреЗрдВрдб рдХрд╣рд▓рд╛рддреЗ рд╣реИред

рд▓рд┐рдЧреЗрдВрдб рдореЗрдВ рдЗрд▓реЗрдХреНрдЯреНрд░рд╛рди рджреЗрдиреЗ рд╡рд╛рд▓рд╛ рдкрд░рдорд╛рдгреБ рджрд╛рддрд╛ рдкрд░рдорд╛рдгреБ рдХрд╣рд▓рд╛рддрд╛ рд╣реИред


1.рдПрдХ рджрдВрддреБрдХ рд▓реАрдЧреЗрдВрдб- рд╡реЗ рд▓рд┐рдЧреЗрдВрдб рдЬрд┐рдирдореЗ рдХреЗрд╡рд▓ рдПрдХ рд╣реА рджрд╛рддрд╛ рд╣реЛрддрд╛ рд╣реИред 


2.рджреНрд╡рд┐ рджрдВрддреБрдХ рд▓рд┐рдЧреЗрдВрдб- рдЬрд┐рдирдореЗ рджреЛ рджрд╛рддрд╛ рдкрд░рдорд╛рдгреБ рд╣реЛред


3. рддреНрд░рд┐рджрдВрддреБрдХ рд▓реАрдЧреЗрдВрдб- рдЬрд┐рдирдореЗ рддреАрди рджрд╛рддрд╛ рдкрд░рдорд╛рдгреБ рд╣реЛред 


4.рдЪрддреБ рджрдВрддреБрдХ рд▓реАрдЧреЗрдб- рдЬрд┐рдирдореЗ рдЪрд╛рд░ рджрд╛рддрд╛  рдкрд░рдорд╛рдгреБ рд╣реЛред


:  рдСрдХреНрд╕реАрдХрд░рдг рд╕рдВрдЦреНрдпрд╛- 

рдирд┐рдпрдо-

1. рдЙрджрд╛рд╕реАрди рд╕рдВрдХреБрд▓ рдореЗрдВ рдХреЗрдВрджреНрд░реАрдп рдзрд╛рддреБ рдкрд░рдорд╛рдгреБ рдУрд░ рд▓рд┐рдЧреЗрдВрдб рдХреЗ рдЖрд╡реЗрд╢реЛрдВ рдХрд╛ рдпреЛрдЧ рд╢реВрдиреНрдп рд╣реЛрддрд╛ рд╣реИред

2.рдСрдХреНрд╕реАрдХрд░рдг рд╕рдБрдЦреНрдпрд╛ рдзрд╛рддреБ рдкрд░рдорд╛рдгреБ рдУрд░ рд▓рд┐рдЧреЗрдВрдбреЛрдВ рдХреЗ рдЖрд╡реЗрд╢реЛрдВ рдХрд╛ рдпреЛрдЧ рд╣реЛрддрд╛ рд╣реИред 


рдЙрджрд╛рд╣рд░рдг-


:рд╣реЛрдореЛрд▓реЗрдкреНрдЯрд┐рдХ рдУрд░ рд╣реЗрдЯреЗрд░реЛрд▓реЗрдкреНрдЯрд┐рдХ рд╕рдВрдХреБрд▓-

  рдЬрд┐рдирдореЗ рджрд╛рддрд╛ рдкрд░рдорд╛рдгреБ рдПрдХ рд╣реА рддрд░рд╣ рдХреЗ рджрд╛рддрд╛ рд╕рдореВрд╣ рд╕реЗ рдЬреБреЬреЗ рд╣реЛрддреЗ рд╣реИ рд╣реЛрдореЛрд▓реЗрдкреНрдЯрд┐рдХ рдХрд╣рд▓рд╛рддреЗ рд╣реИред


рдЬрд┐рдирдореЗ рджрд╛рддрд╛ рдкрд░рдорд╛рдгреБ рдПрдХ рд╕реЗ рдЕрдзрд┐рдХ рдкреНрд░рдХрд╛рд░ рдХреЗ рджрд╛рддрд╛ рд╕рдореВрд╣реЛрдВ рд╕реЗ рдЬреБреЬреЗ рд░рд╣рддреЗ рд╣реИ рд╣реЗрдЯреЗрд░реЛрд▓реЗрдкреНрдЯрд┐рдХ рд╕рдВрдХреБрд▓ рдХрд╣рд▓рд╛рддреЗ рд╣реИред



: рд╕рдордиреНрд╡рдп рдлрд▓рдХ- рдХреЗрдВрджреНрд░реАрдп рдзрд╛рддреБ рд╕реЗ рдЬреБреЬреЗ рд▓рд┐рдЧреЗрдВрдбреЛрдВ рдХреА рд╡реНрдпрд╡рд╕реНрдерд╛ рдХреЛ рд╕рдордиреНрд╡рдп рдлрд▓рдХ рдХрд╣рддреЗ рд╣реИред




Riemer Tiemann reaction

              Reimer Tiemann reaction  Table contents: History About reaction Mechanism Comparasion !> History- Riemer T...