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Ask QuestionPosted by Manish Singh 8 years, 9 months ago
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Posted by Divya Bhaskaran 8 years, 9 months ago
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Posted by Vani Goyal 8 years, 9 months ago
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Pratit Luthra 8 years, 9 months ago
The ability of cation to distort the electron cloud of anion is called polarising power
Posted by Humzah Qadri 8 years, 9 months ago
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Pratit Luthra 8 years, 9 months ago
THAT IS OLIGO SACCHARIDES.
Oligo saccharides are the carbohydrates on hydrolysis give two to ten units of monosaccharides
Posted by Sujeet Kushwaha 8 years, 9 months ago
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Naveen Sharma 8 years, 9 months ago
Ans. Dichlorodiphenyldichloroethylene (DDE) is a chemical compound formed by the loss of hydrogen chloride from DDT, of which it is one of the more common breakdown products.
Posted by Mayank Gupta 8 years, 9 months ago
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Pratit Luthra 8 years, 9 months ago
Because by losing two electrons it attains exactly half filled outermost d orbital
Posted by Harsh Soni 8 years, 9 months ago
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Dr. Kamlapati Bhatt 8 years, 4 months ago
According to the formula oxidation state of N in HNO3 is +5 ,as calculated below.
Let the oxidation state of N be x , then applying the rules to calculate O.N. , we get
+1 +(x) + (- 2 X 3 ) = 0
{tex}\therefore{/tex} x = ( +6 - 1 )
= +5
We know that , N is restricted to a maximum covalency of 4 , since only four (1s and 3p ) orbitals are available for bonding , and also due to the absence of a d-orbital in the atom. However , there are cases where oxidation state of N in compounds like viz . N2 O5 , HNO3 is +5 . This is due to resonating structures of these compounds . Their resonating structures well support and justify the oxidation number of N as +5 in the compound as follows -


Resonating structure of HNO3 results into formation of a coordinate bond , where N donates both the electrons to oxygen atom.
and the double bond is formed with one of the oxygen atoms giving a charge as +2 to N
A single bond with the other oxygen atom gaining a negative charge over it gives a charge of +2 to N
& OH- group gives a charge to N as = +1
Adding up all the charges provided to N in HNO3 ,
Oxidation No. of N in HNO3 = 2+2+1 = 5
similarly the oxidation state of N in N2 O5 can also be made out through its structure as given above.
Posted by Tamanna Bhanwala 8 years, 10 months ago
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Posted by Bhavya Babuta 8 years, 10 months ago
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Posted by Saim Ullah 8 years, 10 months ago
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Bindu Agarwal 8 years, 10 months ago
It is defined as the no. of moles of solute present in 1 L of solution
Posted by Tamanna Bhanwala 8 years, 10 months ago
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Posted by Tamanna Bhanwala 8 years, 10 months ago
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Posted by Shivani Gautam 8 years, 10 months ago
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Bindu Agarwal 8 years, 10 months ago
Catalyst is a substance which can change the speed of the chemical reaction without itself undergoing any change in its mass and chemical composition. and the phenomenon is known as catalysis.
Posted by S Das 8 years, 10 months ago
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Bindu Agarwal 8 years, 10 months ago
In case of p-dichlorobenzene both the chlorine atoms pull the electron cloud towards themseleves woth equal magnitude and in the opposite directiona and hence its dipole moment turns out to be zero while in the case of p dihydroxybenzene O atom is sp3 hybridized and lone pair is not in the plane of the molecule so electron pull is same in magnitude but in different directions hence its dipole moment does not cancel out
Posted by Anu Shka 8 years, 10 months ago
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Posted by Tamanna Bhanwala 8 years, 10 months ago
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Posted by Tamanna Bhanwala 8 years, 10 months ago
- 2 answers
Naveen Sharma 8 years, 10 months ago
Ans. 30 Important Name Reactions are Following :
- Sandmeyer Reaction
- Gatterman Reaction
- Balz-Schiemann Reaction
- Finkelstein Reaction
- Swartz Reaction
- Wurtz Reaction
- Fitting Reaction
- Wurtz - Fittig Reaction
- Kolbe's Reaction
- Reimer- Tiemann Reaction
- Rosenmund Reduction
- Gattermann - Koch Reaction
- Stephen Reaction or Stephen Reduction
- Clemmensen Reduction
- Wolff - Kishner Reduction
- Haloform Reaction (Iodoform Reaction)
- Aldol Condensation
- Cannizzaro Reaction
- Friedel - Crafts Reaction
- Grignard Synthesis
- Esterification Reaction or Fischer Esterification
- Williamson Synthesis
- Diazotisation Reaction
- Etard Reaction
- Hell - Volhard Zelinsky Reaction
- Decarboxylation Reaction
- Hofmann Bromide Reaction
- Gabriel Phthalimide Synthesis
- Coupling Reaction
- Carbylamine Reaction
Posted by Manan Gupta 8 years, 10 months ago
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Naveen Sharma 8 years, 10 months ago
Ans. The radius ratio for AgBr is intermediate. Thus, it shows both frenkel and schottky defects.
The major defect in AgBr is the Frenkel defect. It has a rock salt structure i.e. CCP lattice of Br with atoms of Ag occupying all octahedral holes. Ag moves from octahedral to tetrahedral sites causing only cations to precipitate.
Schottky defect arise due to missing of ions from their lattice point and frenkel arise when the missing ions occupy interstitial sites.
in AgBr, Ag+ ion is small in size and when removed from lattice point they can occupy interstitial site and therefore show both frenkel and schottky defect. SCHOTTKY Defect in AgBr is exhibited due to precipitation of both Cations and Anions.
Posted by Tamanna Bhanwala 8 years, 10 months ago
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Shweta Gulati 8 years, 10 months ago
All these hydrides are covalent in nature and have pyramidal structure. These involve sp3 hybridization of the central atom and one of the tetrahedral positions is occupied by a lone pair.Due to the presence of lone pair, the bond angle in NH3 is less than the normal tetrahedral angle. It has been found to be 107 degrees. Down the group the bond angle decreases as:
In all these hydrides, four electron pairs, three bond pairs and one lone pair surround the central atom. Now, as we move down the group from N to Bi, the size of the atom goes on increasing and its electro negativity decreases. Consequently, the position of bond pair shifts more and more away from the central atom in moving from NH3 to BiH3. For e.g., the bond pair in NH3 is close to N in N-H bond than the bond pair in P-H bond in PH3. As a result, the force of repulsion between the bonded pair of electrons in NH3 is more than in PH3. In general, the force of repulsion between bonded pairs of electrons decreases as we move from NH3 to BiH3 and therefore, the bond angle also decreases in the same order.
Posted by Tamanna Bhanwala 8 years, 10 months ago
- 1 answers
Naveen Sharma 8 years, 10 months ago
Ans. Nitrogen does not have D orbitals whereas Phosphorus on the other hand can expand itself into the d-orbital and thus can share all 5 of it's outer shell electrons.Also Due to small size of Nitrogen, there is a lot of inter-electronic repulsion. So the N-N single bond is very weak.
Posted by Supriya Kumari 8 years, 10 months ago
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Shweta Gulati 8 years, 10 months ago
Make a list of all the questions from these chapters and learn them by heart.
Revise the answers everyday and try to write them too.
Practice these questions thoroughly.
All the best.
Posted by Sunny Dhankhar 8 years, 10 months ago
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Posted by Sanket Chanda 8 years, 10 months ago
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Posted by Keerthi S 8 years, 10 months ago
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Shweta Gulati 8 years, 10 months ago
Aniline is convered to phenyl isocyanide by its reaction with KOH and chloroform i.e. CHCl3
C6H5-NH2 + KOH + CHCI3----------> C6H5-NC
Posted by Keerthi S 8 years, 10 months ago
- 1 answers
Naveen Sharma 8 years, 10 months ago
Ans. Aniline reacts with NaNO2/HCl to form benzenediazonium chloride Which on Reduction with Cu forms Benzene.
Then Benzene reacts with Methyl Chloride in presence of anhydrous AlCl3 Form Toluene.
Toluene in the presence of UV reacts with chlorine atom forms Benzyl Chloride.
Posted by Supriya Kumari 8 years, 10 months ago
- 1 answers
Shweta Gulati 8 years, 10 months ago
It would be better if you solve these questions directly from NCERT.
These chapters have most of the direct questions in paper. And you can refer to the sample papers too.
Learn the most important and most frequent questions from these chapters by heart.
All the best!
Posted by Supriya Kumari 8 years, 10 months ago
- 1 answers
Naveen Sharma 8 years, 10 months ago
Ans. 1) Acetaldehyde to acetone
.bmp)
2) Acetone to Tertabutyl alcohol
.png)
3) Ethyl alcohol to acetone


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