In Dumas' method 292text mg of an organic compound released 50text mL of nitrogen gas (textN_2) at 300text K temperature and 715text mm Hg pressure. [cite: 435, 451] The percentage composition of 'N' in the organic compound is dots % (Nearest integer) [cite: 452, 455] (Aqueous tension at 300text K = 15text mm Hg)

Numerical Answer Type:
Enter a numerical value Answer: 17.5 to 18.5 +4 marks

Solution & Explanation

### Related Formula P_textdry textN_2 = P_texttotal - textAqueous Tension PV = nRT implies n = fracPVRT \%textN = fractextMass of NitrogentextMass of organic compound times 100 ### Core Logic First, isolate the pressure contribution of the dry nitrogen gas: P_textdry textN2 = 715 - 15 = 700text mm Hg = frac700760text atm Using the ideal gas parameters: - V = 50text mL = 0.050text L [cite: 1073, 1076] - T = 300text K - R = 0.0821text L atm mol^-1textK^-1 ### Step 1: Compute Moles and Mass Calculate total moles of textN_2 molecules collected: ntextN2 = fracleft(frac700760 ight) times 0.0500.0821 times 300 approx 1.868 times 10^-3text mol Compute corresponding mass of atomic Nitrogen elements (2 times 14 = 28text g/mol): [cite: 1016, 1017] textMass of N = ntextN2 times 28 = 1.868 times 10^-3 times 28 approx 0.0523text g = 52.3text mg ### Step 2: Calculate Percentage Composition Applying the fraction formulation against total sample mass: [cite: 1021, 1022] \%textN = frac52.3text mg292text mg times 100 approx 17.91\% approx 18\% ### Pattern Recognition Dumas analysis safety check: Always strip away the vapor pressure of water (aqueous tension) from the measured barometric value before computing the chemical molar counts. For standard conditions shortcuts, remember that 1text mole = 22400text mL at STP can act as an alternate path if values are normalized. ### 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

More Organic Chemistry - Some Basic Principles and Techniques Questions — jee_main_2025_07_april_evening

Practice all Organic Chemistry - Some Basic Principles and Techniques previous-year questions →

Rankbit System
JEE Physics: Waves (+15.5%) | Electrostatics: Concentric Shells (-29.7%) | Modern Physics: Photoelectric Clones (+34.2%) | Mathematics: Definite Integrals (+18.1%) | Chemistry: Coordination Splitting (-11.4%) | JEE Physics: Waves (+15.5%) | Electrostatics: Concentric Shells (-29.7%) | Modern Physics: Photoelectric Clones (+34.2%) | Mathematics: Definite Integrals (+18.1%) | Chemistry: Coordination Splitting (-11.4%)