BIT Mesra All Questions

Hello,
Why you want to re-upload.Just click on submit button and confirm your application form and do the payment process and if you face any other problems then contact the concerned department.
Good luck.

Hi Aspirant,
Here,the syllabus is provided in full detail:-
Concepts
Hybridisation of carbon; Sigma and pi-bonds; Shapes of simple organic molecules; Structural and geometrical isomerism; Optical isomerism of compounds containing up to two asymmetric centres, (R,S and E,Z nomenclature excluded); IUPAC nomenclature of simple organic compounds (only hydrocarbons, mono-functional and bi-functional compounds); Conformations of ethane and butane (Newman projections); Resonance and hyperconjugation; Keto-enol tautomerism; Determination of empirical and molecular formulae of simple compounds (only combustion method); Hydrogen bonds: definition and their effects on physical properties of alcohols and carboxylic acids; Inductive and resonance effects on acidity and basicity of organic acids and bases; Polarity and inductive effects in alkyl halides; Reactive intermediates produced during homolytic and heterolytic bond cleavage; Formation, structure and stability of carbocations, carbanions and free radicals
Preparation, properties and reactions of Alkenes
Homologous series, physical properties of alkanes (melting points, boiling points and density); Combustion and halogenation of alkanes; Preparation of alkanes by Wurtz reaction and decarboxylation reactions
Preparation, properties and reactions of alkenes and alkynes
Physical properties of alkenes and alkynes (boiling points, density and dipole moments); Acidity of alkynes; Acid catalysed hydration of alkenes and alkynes (excluding the stereochemistry of addition and elimination); Reactions of alkenes with KMnO4 and ozone; Reduction of alkenes and alkynes; Preparation of alkenes and alkynes by elimination reactions; Electrophilic addition reactions of alkenes with X2, HX, HOX and H2O (X=halogen); Addition reactions of alkynes; Metal acetylides
Reactions of benzene: Structure and aromaticity; Electrophilic substitution reactions
halogenation, nitration, sulphonation, Friedel-Crafts alkylation and acylation; Effect of o-, m- and p-directing groups in monosubstituted benzenes.
Phenols
Acidity, electrophilic substitution reactions (halogenation, nitration and sulphonation); Reimer-Tieman reaction, Kolbe reaction.
Characteristic reactions of the following (including those mentioned above)
Alkyl halides: rearrangement reactions of alkyl carbocation, Grignard reactions, nucleophilic substitution reactions; Alcohols: esterification, dehydration and oxidation, reaction with sodium, phosphorus halides, ZnCl2/concentrated HCl, conversion of alcohols into aldehydes and ketones
Characteristic reactions of the following (including those mentioned above)
Alkyl halides: rearrangement reactions of alkyl carbocation, Grignard reactions, nucleophilic substitution reactions; Alcohols: esterification, dehydration and oxidation, reaction with sodium, phosphorus halides, ZnCl2/concentrated HCl, conversion of alcohols into aldehydes and ketones; Ethers:Preparation by Williamson's Synthesis; Aldehydes and Ketones: oxidation, reduction, oxime and hydrazone formation; aldol condensation, Perkin reaction; Cannizzaro reaction; haloform reaction and nucleophilic addition reactions (Grignard addition); Carboxylic acids: formation of esters, acid chlorides and amides, ester hydrolysis; Amines: basicity of substituted anilines and aliphatic amines, preparation from nitro compounds, reaction with nitrous acid, azo coupling reaction of diazonium salts of aromatic amines, Sandmeyer and related reactions of diazonium salts; carbylamine reaction; Haloarenes: nucleophilic aromatic substitution in haloarenes and substituted haloarenes (excluding Benzyne mechanism and Cine substitution).
Carbohydrates
Classification; mono- and di-saccharides (glucose and sucrose); Oxidation, reduction, glycoside formation and hydrolysis of sucrose.
Amino acids and peptides: General structure (only primary structure for peptides) and physical properties.
Properties and uses of some important polymers: Natural rubber, cellulose, nylon, teflon and PVC.

This was what to study.
Now,how to study.
Theory comes first.Make sure that you have all the reactions,reagents and conversions at the tip of your tongue.
When we get through this (which shall take 40% of your time),spend the rest of the time solving questions from the books you've mentioned.
All of them are quality books and contain a large number of questions suited to prepare you well for JEE.
Hope this helps.

Hello Dear

Inorder check the Mock test for JEE MAINS examination. You can also visit this below link to check the sets of unsolved question of JEE Mains.

https://engineering.careers360.com/articles/jee-main-mock-test/amp

All the best

Hello Aspirant,


You can get admission in BiT mesra for MBA.You can apply through their official website or you can reach out the college.

I hope this helps.

Both are the good options but if you have completed your Graduation in Industrial Chemistry then you should go for Industrial Chemistry because you are already well known with the subjects. It has also a good scope if you are pursuing the course from a recognised university the chances of you getting a good position in the industry is good. You have the option for an industrial job or into the research field. If you plan to go the industrial side you can opt for manufacturing unit, Production and development units etc. If you are interested in the research area you can opt for going in for PH.d. Along with pursuing PHD you can opt for joining a laboratory or a research unit. This will help you in your PHD too. But you need to work hard to get a position.

Good Luck!