Did edit window open??
Did edit window open??
Did edit window open??
Guys what all is visible to you in freshers portal could someone update below
When does the hostel dees and allocation prcess start for freshers and when is the orientation and date of start of classes further more if we want to with draw we will also get the hostel fees refunded right
Can we prepay sbi scholar loans
Is ECE at IIIT DHARWAD worth it over vit vellore cse
Guys I forgot to upload my class 12 marksheet during preference form filling please tell if I can upload in the future????
Seniors do we pay for hostel at the vit vellore campus or in the freshers portal a month before
Could any seniors give me a timeline and process for internships of dual degree holders. I my understanding they dont have ps1 but have s1 and ps2 also what do these signify like what do these particular intenships entail like no pay etc???
So how stressfull is it and what percentage of stu get mnc or cse allotted. Also how many extra courses per sem for a dual degree student.
Please advise me on this seniors
Could you please clarify the dual-degree allotment process for MSc students? My understanding is that students can opt for a dual degree at the end of their second semester, with course availability being determined by their first-year CGPA. Is this correct?
Also Does anybody have branch cutoffs for BE allotment of last year in BITS Hyd Campus
Guys 100 percent some kind of cheating happened this year because the data seems so anomalous and impossible
Guys feel like mathongo ke ranges ke waja se 5 to 9 makrs increase hue hai from my friend it went from 170 to 179 in math ongo so after officail key sabke niche jayenge also i think the data has almost reached peak saturation
ALSO WE ARE HAVING 8864 STUDENTS ABOVE 100 SO EVEN IFF WE DOUBLE IT LOOKS LIKE 2025 but obviously it will not be double ad midrange data is skewed so take it as 1.5 to 1.7 about the nos of people above you
(5737+3016+1409+568+232+81+29+4)×1.5=16,614
This list covers the most essential common names in organic chemistry, specifically those frequently used in identification tests, stoichiometry, and naming problems (like JEE, NEET, and Olympiads).
These are crucial for stoichiometry problems involving neutralization and esterification.
| Common Name | IUPAC Name | Formula | Notes |
|---|---|---|---|
| Formic Acid | Methanoic acid | $ce{HCOOH}$ | Reduces Tollens' reagent (unique for an acid). |
| Acetic Acid | Ethanoic acid | $ce{CH3COOH}$ | Found in Vinegar. |
| Oxalic Acid | Ethanedioic acid | $ce{(COOH)2}$ | Used in redox titrations with $ce{KMnO4}$. |
| Malonic Acid | Propanedioic acid | $ce{CH2(COOH)2}$ | Forms a cyclic anhydride easily. |
| Succinic Acid | Butanedioic acid | $ce{(CH2)2(COOH)2}$ | Key in the Krebs cycle. |
| Adipic Acid | Hexanedioic acid | $ce{(CH2)4(COOH)2}$ | Monomer for Nylon-6,6. |
| Lactic Acid | 2-Hydroxypropanoic acid | $ce{CH3CH(OH)COOH}$ | Found in sour milk; contains a chiral center. |
| Malic Acid | Hydroxybutanedioic acid | $ce{HOOC-CH(OH)-CH2-COOH}$ | Found in apples. |
| Tartaric Acid | 2,3-Dihydroxybutanedioic acid | $ce{[CH(OH)COOH]2}$ | Used in Fehling's solution (as Rochelle salt). |
| Citric Acid | 2-hydroxypropane-1,2,3-tricarboxylic acid | $ce{C6H8O7}$ | A tricarboxylic acid found in citrus. |
Commonly used in Ferric Chloride tests and Coupling reactions.
| Common Name | Description | Structure |
|---|---|---|
| Phenol | Carbolic acid | $ce{C6H5OH}$ |
| Catechol | 1,2-Dihydroxybenzene | Ortho-isomer |
| Resorcinol | 1,3-Dihydroxybenzene | Meta-isomer |
| Quinol (Hydroquinone) | 1,4-Dihydroxybenzene | Para-isomer (used as developer) |
| Pyrogallol | 1,2,3-Trihydroxybenzene | Absorbs alkaline oxygen. |
| Phloroglucinol | 1,3,5-Trihydroxybenzene | Used in testing lignin. |
| o-Cresol | 2-Methylphenol | Ortho-methyl phenol. |
| Picric Acid | 2,4,6-Trinitrophenol | Highly acidic despite no $ce{-COOH}$ group. |
Crucial for Cannizzaro and Perkin reactions.
| Common Name | IUPAC/Description | Formula/Structure |
|---|---|---|
| Benzaldehyde | Benzenecarbaldehyde | $ce{C6H5CHO}$ |
| Salicylaldehyde | 2-Hydroxybenzaldehyde | Product of Reimer-Tiemann reaction. |
| Benzoic Acid | Benzenecarboxylic acid | $ce{C6H5COOH}$ |
| Salicylic Acid | 2-Hydroxybenzoic acid | Precursor to Aspirin. |
| Phthalic Acid | Benzene-1,2-dicarboxylic acid | Ortho-isomer. |
| Isophthalic Acid | Benzene-1,3-dicarboxylic acid | Meta-isomer. |
| Terephthalic Acid | Benzene-1,4-dicarboxylic acid | Used in making Terylene/Dacron. |
| Cinnamic Acid | 3-phenylprop-2-enoic acid | $ce{C6H5-CH=CH-COOH}$ |
Important for Ozonolysis and addition stoichiometry.
| Common Name | IUPAC Name | Formula |
|---|---|---|
| Acrolein | Prop-2-enal | $ce{CH2=CH-CHO}$ |
| Crotonaldehyde | But-2-enal | $ce{CH3-CH=CH-CHO}$ |
| Vinyl Alcohol | Ethenol | $ce{CH2=CHOH}$ (Unstable, tautomerizes) |
| Allyl Alcohol | Prop-2-en-1-ol | $ce{CH2=CH-CH2OH}$ |
| Maleic Acid | cis-Butenedioic acid | cis-isomer (forms anhydride easily). |
| Fumaric Acid | trans-Butenedioic acid | trans-isomer (high melting point). |
Used in Carbylamine and Hinsberg tests.
| Common Name | IUPAC/Description | Notes |
|---|---|---|
| Aniline | Benzenamine | Primary aromatic amine. |
| Acetanilide | N-phenylacetamide | Used to protect aniline group. |
| Urea | Aminoformamide | $ce{NH2CONH2}$ (First synthesized organic compound). |
| Pyridine | Azabenzene | $ce{C5H5N}$ (Basic heterocyclic compound). |
| Pyrrole | Azole | 5-membered heterocyclic ring. |
| Glycine | 2-aminoethanoic acid | Simplest amino acid (not chiral). |
To remember the sequence of $\ce{-(CH2)_n-}$ between the two $\ce{-COOH}$ groups: "Oh My Such Good Apple Pie"
Below is the exhaustive list of compounds that react with Tollens' and Fehling's reagents, including the necessary stoichiometry for calculations.
| Compound Class | Specific Examples | Tollens' (Ag Mirror) | Fehling's (Red Ppt) | Stoichiometry (Reactant : Ag or $Cu_2O$) |
|---|---|---|---|---|
| Aliphatic Aldehydes | Formaldehyde, Ethanal | (+) | (+) | 1 : 2 Ag / 1 : 1 $Cu_2O$ |
| Aromatic Aldehydes | Benzaldehyde | (+) | (-) | 1 : 2 Ag |
| $alpha$-Hydroxy Ketones | Fructose, Acetoin | (+) | (+) | 1 : 2 Ag / 1 : 1 $Cu_2O$ |
| Formic Acid | $HCOOH$ | (+) | (+) | 1 : 2 Ag / 1 : 1 $Cu_2O$ |
| Reductones | Ascorbic Acid (Vit C) | (+) | (+) | 1 : 2 Ag / 1 : 1 $Cu_2O$ |
| Hydrazines | Phenylhydrazine | (+) | (+) | 1 : 4 Ag / 1 : 2 $Cu_2O$ |
| Hydroxylamines | $R-NHOH$ | (+) | (+) | 1 : 2 Ag / 1 : 1 $Cu_2O$ |
| Polyhydroxy Phenols | Hydroquinone, Catechol | (+) | (-) | 1 : 2 Ag |
| Terminal Alkynes | Ethyne, Propyne | (+)* | (-) | 1 : 1 Ag-acetylide (Ppt) |
Formic acid is the only carboxylic acid to give these tests because the Carbon-Hydrogen bond attached to the carboxyl group acts like an aldehyde.
These react because they undergo Lobry de Bruyn–van Alberda van Ekenstein transformation in the basic medium of the reagents to form aldehydes.
Hydrazines are very powerful reducing agents. Phenylhydrazine is often used in carbohydrate chemistry (Osazone formation) and will reduce Tollens' reagent to silver.
Used in photography as "developers" precisely because they reduce silver ions to metallic silver.
The enediol structure is highly sensitive to oxidation.
If you are given a mass of "Silver Mirror" or "Red Precipitate" and asked to identify or quantify the organic compound:
Note on $\alpha,\beta$-unsaturated ketones: If you encounter a problem where an unsaturated ketone gives a positive test, look closely at the structure. If it is an $\alpha,\beta$-unsaturated aldehyde (like Acrolein), it is (+). If it is a ketone with an $-\text{OH}$ group on the adjacent carbon, it is (+). Otherwise, simple ketones are consistently negative.
So b/w vit vellore cat 2 cse and mu which is better for cse and job placements any suggestions guys
Disregard roi What about mu scholarship as i have 96 percentile above in jee mains
20xx can someone guide me regd choice filling pls like can i get cse core cat 1 or only 2