In Dumas' method for estimation of nitrogen, 1mathrm~g of an organic compound gave 150mathrm~mL of nitrogen collected at 300mathrm~K temperature and 900mathrm~mmHg pressure. The percentage composition of nitrogen in the compound is _______ % (nearest integer). (Aqueous tension at 300mathrm~K = 15mathrm~mmHg)

Numerical Answer Type:
Enter a numerical value Answer: 20 to 20 +4 marks

Solution & Explanation

### Related Formula P_textdry N_2 = P_texttotal - P_textaqueous tension PV = nRT implies n = fracPVRT \% N = fractextMass of NitrogentextMass of Organic Compound times 100 ### Core Logic First, calculate the actual pressure exerted by the dry nitrogen gas: P_N_2 = 900 - 15 = 885mathrm~mmHg = frac885760mathrm~atm Convert volume data to liters: V = 150mathrm~mL = 0.15mathrm~L. Using the ideal gas law to determine the moles of N_2 collected: n = fracleft(frac885760right) times 0.150.0821 times 300 = frac1.1645 times 0.1524.63 approx 0.0071mathrm~moles Calculate the total mass of the liberated nitrogen gas: textMass = n times M_textmolar = 0.0071 times 28 = 0.1988mathrm~g Determine the percentage composition relative to the initial 1mathrm~g sample size: \% N = frac0.19881 times 100 = 19.88\% approx 20\% ### Pattern Recognition Always remember to subtract the aqueous tension value first. Failing to correct for water vapor pressure is the most common pitfall in Dumas' method calculations. ### Evaluation Rubric / Model Answer null ### Chapter Mix Class 11 Chemistry: Organic Chemistry - Some Basic Principles and Techniques

Reference Study Guides

More Organic Chemistry - Some Basic Principles and Techniques Previous-Year Questions — Page 12

Q62 jee_main_2024_27_jan_morning Isomerism
  • A. Structure A
  • B. Structure B
  • C. Structure C
  • D. Structure D

Solution

### Core Logic The enol form of structure (2) produces a fully conjugated, aromatic ring system (phenol derivative) which provides immense resonance stabilization. Therefore, the equilibrium lies heavily toward the enol form.
Enol conversion pathway diagram for Q62 - JEE Main 2024 Morning
Four choices depicting structure inputs for keto compounds tautomerizing to enols.
### Pattern Recognition Look for enol forms that attain aromaticity. Aromatic stabilization overrides typical keto-preference factors. ### Chapter Mix Class 11 Chemistry: Organic Chemistry - Some Basic Principles and Techniques
Q64 jee_main_2024_27_jan_morning Basic Strength
Which of the following is strongest Bronsted base?
  • A. Option 1
  • B. Option 2
  • C. Option 3
  • D. Option 4

Solution

### Core Logic Option (4) is a cyclic secondary aliphatic amine (piperidine derivative) where the nitrogen atom is textsp^3 hybridized and its lone pair is entirely localized, making it highly available to accept a proton. In contrast, options (1), (2), and (3) have lone pairs involved in resonance with aromatic systems or unsaturated structures.
Lone pair localization logic diagram for Q64 - JEE Main 2024 Morning
Four different amine ring structures listed as options.
### Pattern Recognition Localized aliphatic amines are consistently stronger Bronsted bases than aromatic or delocalized analogs. ### Chapter Mix Class 11 Chemistry: Organic Chemistry - Some Basic Principles and Techniques
Q66 jee_main_2024_27_jan_morning Acidic Strength
Which of the following has highly acidic hydrogen?
  • A. Structure 1
  • B. Structure 2
  • C. Structure 3
  • D. Structure 4

Solution

### Core Logic Option (4) features an active methylene group flanked directly between two electron-withdrawing carbonyl groupings. The removal of a proton from this central -textCH_2- carbon produces a conjugate base that is strongly stabilized via extensive delocalization across both oxygen atoms.
Conjugate base stabilization resonance scheme for Q66 - JEE Main 2024 Morning
Four carbonyl organic structures presented as options.
### Pattern Recognition Look for hydrogens between two -M / -I carbonyl complexes rightarrow Active methylene effect. ### Chapter Mix Class 11 Chemistry: Organic Chemistry - Some Basic Principles and Techniques
Q74 jee_main_2024_27_jan_morning Classification of Organic Compounds
Cyclohexene is textquadquad type of an organic compound.
  • A. Benzenoid aromatic
  • B. Benzenoid non-aromatic
  • C. Acyclic
  • D. Alicyclic

Solution

### Core Logic Cyclohexene features an aliphatic carbon ring framework containing an unsaturated double bond but lacks an aromatic sextet ring structure. It belongs to the alicyclic category (aliphatic + cyclic compounds).
Cyclohexene chemical ring diagram for Q74 - JEE Main 2024 Morning
Cyclohexene chemical ring diagram for Q74 - JEE Main 2024 Morning
### Chapter Mix Class 11 Chemistry: Organic Chemistry - Some Basic Principles and Techniques
Q77 jee_main_2024_27_jan_morning IUPAC Nomenclature
IUPAC name of following compound (P) is:
Substituted ring framework structural layout for Q77 - JEE Main 2024 Morning
Substituted cyclohexane molecule labeled as compound P.
Substituted ring framework structural layout for Q77 - JEE Main 2024 Morning
Substituted cyclohexane molecule labeled as compound P.
  • A. 1-Ethyl-5, 5-dimethylcyclohexane
  • B. 3-Ethyl-1,1-dimethylcyclohexane
  • C. 1-Ethyl-3, 3-dimethylcyclohexane
  • D. 1,1-Dimethyl-3-ethylcyclohexane

Solution

### Core Logic Number the ring to give substituents the lowest possible locants. Setting locant 1 at the carbon carrying the two methyl groups provides a locant list of (1,1,3), whereas setting it at the ethyl-bearing carbon gives (1,3,3). The set (1,1,3) wins by the lowest locant rule. Then arrange alphabetically: 3-ethyl precedes 1,1-dimethyl. Hence, the correct systematic tag is 3-Ethyl-1,1-dimethylcyclohexane.
Locant indexing direction chart for Q77 - JEE Main 2024 Morning
Substituted cyclohexane molecule labeled as compound P.
### Pattern Recognition Lowest locant grouping set takes ultimate priority before checking alphabetical organization rules. ### Chapter Mix Class 11 Chemistry: Organic Chemistry - Some Basic Principles and Techniques

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