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UPSC Previous Year Question Paper 2026 – Combined Geo-Scientist (Main) Examination | SNCS-A-CMS Chemistry Paper-III | Free PDF Download
UPSC Previous Year Question Paper 2026 – Combined Geo-Scientist (Main) Examination | SNCS-A-CMS Chemistry Paper-III | Free PDF Download
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Combined Geo- Scientist (Main) Examination, 2026
CHEMISTRY
PAPER- III
Time Allowed : Three Hours
Maximum Marks : 200
QUESTION PAPER SPECIFIC INSTRUCTIONS
Please read each of the following instructions carefully before attempting questions
There are TEN questions divided under TWO Sections.
Candidate has to attempt SIX questions in all.
Question No. 1 in Section- A and Question No. 6 in Section- B are compulsory. Of the remaining questions, candidates have to answer FOUR questions, choosing TWO from each Section.
The number of marks carried by a question/part is indicated against it.
Neat sketches are to be drawn to illustrate answers, wherever required. These shall be drawn in the space provided for answering the question itself.
Unless otherwise mentioned, symbols and notations have their usual standard meanings.
Assume suitable data, if necessary, and indicate the same clearly.
Attempts of questions shall be counted in sequential order. Unless struck off, attempt of a question shall be counted even if attempted partly.
Any page or portion of the page left blank in the Question- cum- Answer (QCA) Booklet must be clearly struck off.
Answers must be written in ENGLISH only.
UPSC Previous Year Question paper , NCS-A-CMS Chemistry Paper-III, Free PDF Download, Combined Geo-Scientist, UPSC Previous Year Question Paper 2026,
Combined Geo-Scientist (Main) Examination, 2026
SNCS-C-CMS
CHEMISTRY
PAPER—III Time Allowed : Three Hours
Maximum Marks : 200 QUESTION PAPER SPECIFIC INSTRUCTIONS Please read each of the following instructions carefully before attempting questions There are TEN questions divided under TWO Sections.
Candidate has to attempt SIX questions in all.
Question No. 1 in Section—A and Question No. 6 in Section—B are compulsory. Of the remaining questions, candidates have to answer FOUR questions, choosing TWO from each Section.
The number of marks carried by a question/part is indicated against it.
Neat sketches are to be drawn to illustrate answers, wherever required. These shall be drawn in the space provided for answering the question itself.
Unless otherwise mentioned, symbols and notations have their usual standard meanings.
Assume suitable data, if necessary, and indicate the same clearly.
Attempts of questions shall be counted in sequential order. Unless struck off, attempt of a question shall be counted even if attempted partly.
Any page or portion of the page left blank in the Question-cum-Answer (QCA) Booklet must be clearly struck off.
Answers must be written in ENGLISH only. SECTION—A (a) A geologist received certain samples as follows :
Sample | Weight of sample (g)
Sample 1 | 2.50 x 10^-1
Sample 2 | 2.40 x 10^-3
Sample 3 | 5.00 x 10^-5
Sample 4 | 1.50 x 10^-2
Sample 5 | 7.00 x 10^-5
Sample 6 | 1.75 x 10^-3
Sample 7 | 0.75 x 10^-1
Classify the above samples as per their respective sample size following the sampling protocol for analytical chemist. (5) (b) In gas chromatography, what is the effect of stationary-phase film thickness on gas chromatograms? (5) (c) An amine sample is analyzed as the picrate derivative. A 0.05 g sample is reacted with picric acid and diluted to 1 L deionized water. The solution exhibits an absorbance of 0.40 in a 1 cm cell. What is the percentage of amine in the sample?
[lambda_max = 359 nm; epsilon = 1.25 x 10^4 cm^-1 mol^-1 L; formula weight of the amine = 310] (5) (d) What is the principle used in VG-AAS? Give the names of two elements that are measured with better detection limit using VG-AAS than by flame AAS. (5) (e) Name three gases used for purging in thermogravimetric analysis (TGA). Justify your answer. (5) (f) What is the cause of fluorescence in X-ray diffraction? How does fluorescence phenomenon impact X-ray diffraction data? (5) (g) (i) What is the purpose of using argon gas in ICPMS? (2)
(ii) Why is HCl or HClO4 not recommended for sample preparation for arsenic analysis by ICPMS? (3) upsc previous year question paper civil service combined Geo Scientist main Examination Chemistry III(h) A solution comprising 1.0 g pyrolusite is treated with 100 mL of 0.1 N oxalic acid and H2SO4. The excess oxalic acid requires 27 mL of 0.05 N KMnO4 for complete titration. Find the amount of MnO2 (in wt%) in the sample.
[Given: Molar mass of MnO2 = 87 g mol^-1] (5) (a) The first three peaks in an X-ray diffractogram (XRD) of metal M are obtained at 2theta values of 38.6°, 55.7° and 70.0°, using Cu Kalpha radiation (lambda = 1.542 A).
Compare the crystal structure and atomic radii with those given in the table below, and identify M:
Metal | Crystal structure | Atomic radius (A)
Al | FCC | 1.431
Au | FCC | 1.442
Pt | FCC | 1.387
Cr | BCC | 1.249
Mo | BCC | 1.363
Ta | BCC | 1.429
Ti | HCP | 1.445
Zn | HCP | 1.332
Cd | HCP | 1.490 (15) (b) (i) Why is quantitative analysis of Fe2+ by spectrophotometric method drastically improved by complexation with 1,10-phenanthroline? What analytical parameters are improved? (3+4)
(ii) How will you validate the above method of analysis? (3) (c) How can the age of a geological deposit be determined by ICPMS analysis? (5) (a) Aluminium (Al) content (in g) in a 100 g bauxite sample is determined by two different laboratory methods, as given below:
Sl. No. | Method-A | Method-B | 51.0 | 51.1 | 51.9 | 52.0 | 52.3 | 52.7 | 54.4 | 54.6 | 50.9 | 51.2 | 53.1 | 53.4
Calculate the 'variance' of the analyses by both methods (A and B) above and compare their precision through F-test, and state which of the methods, A or B, is significant for analysis of Al in bauxite ore.
[F-table is provided in the next page] (10) F-table (Probability level, Phi_2, Phi_1 values provided for 0.10, 0.05, 0.01 across degrees of freedom 1 to infinity) (b) The following data is given for Fe analysis by atomic absorption spectrometry :
Concentration of Fe (mg/L) | Instrument response (absorbance)
0.000 | 0.040
2.000 | 0.150
5.000 | 0.380
15.000 | 1.020
Unknown | 0.832
The least square fit of the calibration data is given as y = 0.064x + 0.032.
(i) Can we estimate Fe in a sample with concentration 0.200 mg/L? Explain.
(ii) Determine the concentration of Fe in the unknown sample.
[Given : The blank sample was measured for 25 times and the standard deviation of the mean value (i.e., 0.040) is 0.008] (6+4) upsc previous year question paper civil service combined Geo Scientist main Examination Chemistry III(c) A sample of petroleum distillate during Doctor Test is shaken with a faint yellow colour solution X. No change in colour is observed. Then some sulphur is added and the solution turns dark brown. This happens when Y species is present in a petroleum distillate. What are X and Y? (2+3) (d) Calculate the resolution of two analytes, whose chromatographic peaks are separated by 4 min with bandwidth of each analyte as 0.5 min. (5) (a) Describe how the ion-exchange capacity of an anion-exchange resin can be measured using standard NaOH, standard HCl or any other reagent. (10) (b) In the thermogravimetric analysis (TGA) of 0.45 g of Ca(OH)2 sample, the losses in weight at different temperatures are as follows :
(i) 0.025 g at 100 °C-150 °C
(ii) 0.040 g at 500 °C-560 °C
(iii) 0.023 g at 900 °C-950 °C
What is the composition of calcium hydroxide in the sample? (10) (c) Using the following data, find the difference between gross calorific value and net calorific value of a coal sample whose composition (by weight) is carbon = 85.0%, hydrogen = 10.29% and ash = 4.71%
Data:
Mass of the coal sample fired in a bomb calorimeter = 1.5 g
Mass of water taken in the calorimeter = 2500 g
Mass equivalent of the calorimeter = 2750 g
Rise in temperature in the calorimeter = 3.0 °C
Specific heat of water = 1 cal/(g °C)
Latent heat of condensation of steam = 540 cal/g
Assume all correction factors to be negligible. (10) (a) Interference filters are used as wavelength selectors. Sketch a typical interference filter and explain how interference filters provide narrow band of radiation. (10) (b) An organic acid dissolved in 50 mL of water is equilibrated with 50 mL of ether. The distribution coefficient (KD) is 50 and the dissociation constant (Ka) is 5.0 x 10^-5. Calculate the distribution ratio (D), if the aqueous layer is at pH 3, pH 5 and pH 7. (10) (c) How will Cu content in a brass sample be quantitatively analyzed volumetrically without interference from Zn present? Describe the method and steps involved in the analysis. (10) upsc previous year question paper civil service combined Geo Scientist main Examination Chemistry IIISECTION—B (a) Predict the major product in the following reactions, and name the reactions:
(i) Ph-CONH2 + Br2 / KOH -> ?
(ii) Cyclohexanone + NaN3, H2SO4 / CH3Cl -> ? (2+2) (b) Identify the major products in the given reactions:
(i) Ph-CHO + KOH / heat -> A + B
(ii) (CH3)2CH-C(CH3)2-CO2C2H5 + LiAlH4 / THF -> C
(iii) Cyclohex-2-enone-derived compound / ester/nitrile + Ca(BH4)2 -> D (4) (c) Identify the major product (X) formed in the following reaction sequence and suggest a suitable mechanism for the conversion of X -> Y:
Indole + CH2O + Me2NH / CH3CO2H -> X
X + NaCN / H2O -> Y (3-(cyanomethyl)indole) (4) (d) Predict the reactants and identify the name of the reactions in the following:
(i) A + B + NaCN, EtOH -> Benzoin derivative
(ii) C + D + t-BuOK, t-BuOH -> alpha,beta-unsaturated ester (2+2) (e) Identify the major products A and B formed in the following reactions:
Enone + mCPBA -> A
Enone + H2O2 / NaOH -> B (2+2) (f) Predict the major products (A-C) formed (with appropriate stereochemistry, if any) in the following reaction sequence:
Biphenyl / cis-stilbene photocyclization: reactant + hnu -> A; A + hnu -> B; B + I2 -> C (4) (g) The optically active compound (X) racemizes on heating. Explain the observation :
[Optically active chiral bicyclic/diene hydrocarbon X] (4) (h) In IR spectrum, the selected bands observed for the unknown amide having molecular formula C4H9NO are 3350, 3200, 2925, 1660 and 1420 cm^-1. Among the following, identify the amide that gives the observed bands and justify your answer:
A: Butanamide (primary amide)
B: Secondary amide
C: Tertiary amide (4) (i) Using Woodward-Fieser rule, calculate lambda_max for the following compounds and arrange them in the order of increasing lambda_max:
Diene compounds A, B, and C with methyl substituents and ring residues (4) (j) The unknown dihaloalkane gives a molecular ion peak at m/z = 128 with a relative intensity of 75. The relative intensities of M+2 and M+4 peaks are 100 and 25 respectively. Identify the halides present in the compound and justify your answer. (4) upsc previous year question paper civil service combined Geo Scientist main Examination Chemistry III(a) Predict the major products (A-C) formed (with appropriate stereochemistry, if any) in the following reaction sequence. Describe the mode of cyclization involved under thermal and photochemical conditions:
Triene / conjugated polyene system: heat -> A; hnu -> B; heat -> C (10) (b) (i) 1H NMR spectrum of bullvalene (X) shows a single signal at delta 4.22 ppm at 100 °C. Explain the observation: (5)
(ii) Suggest a suitable reaction mechanism for the following reaction:
N,N-dimethyl hydrazinium salt derivative + NaOH -> Cyclized alcohol product + Me3N (5) (c) (i) Identify the product and provide the name and mechanism for the following reaction:
Benzoic acid + Na, liq. NH3 / ROH -> ? (5)
(ii) Predict the major products X and Y formed in the following reaction sequence. Suggest a suitable mechanism for the formation of X:
Diethyl malonate + Benzalacetone + NaOEt / EtOH -> X; X + NaOH, H2O / heat -> Y (5) (a) In a solution, acetylacetone exhibits keto-enol tautomerism. The chemical shift (delta in ppm) and their intensity observed in the 1H-NMR of acetylacetone in CDCl3 is given below.
[O-H signal of the enol tautomer is not shown]
delta (in ppm) | Intensity
5.52 | 360
3.61 | 90
2.24 | 270
2.04 | 2160
(i) Assign the signals to the corresponding hydrogen in the tautomers.
(ii) Calculate the ratio of keto-enol tautomers and identify the major tautomer present in the solution. (10) (b) (i) Draw the pi-molecular orbitals of 1,3-butadiene and arrange them in the order of their energy. Assign the HOMO and LUMO under thermal and photochemical conditions. (5)
(ii) Arrange the following dienes in the increasing order of reactivity towards maleic anhydride. Explain your answer:
A: cis-diene isomer
B: trans-diene isomer
C: substituted diene isomer (5) (c) (i) The major product formed on ethyl propionate with KOH in ethanol gives a strong C=O stretching frequency at 1745 cm^-1 and 1725 cm^-1 in IR spectrum. Identify the major product and suggest the suitable mechanism. (5)
(ii) The unknown monoterpene on complete reductive ozonolysis with O3 and Me2S gave equimolar mixture of formaldehyde, acetone, pyruvaldehyde and malondialdehyde. Draw the structure of all the products and deduce the structure of the monoterpene. (5) upsc previous year question paper civil service combined Geo Scientist main Examination Chemistry III(a) Draw the major products formed in the following reactions and describe the process involved :
(i) Vinyl allyl ether derivative + heat -> X (Claisen rearrangement)
(ii) Sulfoxide elimination / Sigmatropic rearrangement: PhS-derivative + heat -> Y; Y + heat -> Z (10) (b) (i) Among the following, identify the ionone that will give the peak at m/z = 136 in EI mass spectrum and explain your answer:
alpha-ionone vs beta-ionone (5)
(ii) Draw the major products (A-C) formed (with appropriate stereochemistry, if any) in the following reaction sequence:
Phosphonate + PhCHO + NaH, THF -> A (Horner-Wadsworth-Emmons)
A + DIBAL-H (2 equiv.), THF -> B (reduction to allylic alcohol)
B + Ti(OiPr)4, (+)-DET, t-BuOOH -> C (Sharpless epoxidation) (5) (c) Propose the mechanism for polymerization of alkene C2H4 when treated with Ziegler-Natta catalyst. Predict the nature of conductivity of the formed polymer and justify your answer. (10) (a) An organic compound having molecular formula C10H16O4 gave the following spectral data:
IR: Significant absorption bands at 2904, 1725, 1641, 1244 cm^-1
1H NMR (400 MHz, CDCl3): delta 4.23 (q, J = 7.2 Hz, 4 H), 2.06 (s, 6 H) and 1.29 (t, J = 7.2 Hz, 6 H)
13C NMR (100 MHz, CDCl3): delta 165.7, 154.9, 124.8, 60.8, 23.1 and 14.1
EI-MS: Prominent peaks at m/z 99 and 155
Deduce the structure of the compound and explain the data. (10) (b) (i) Suggest a suitable method for the synthesis of the following compound (Z) from cyclopentadiene:
[Norbornadiene / bicyclic derivative Z] (5)
(ii) Identify the major products (X-Z) formed in the following reaction sequence:
Alkene hydroboration: Alkene + BH3 -> X; X + PhCHO / NaOH -> Z (5) (c) (i) Predict the major product in the given reaction with possible mechanism. Also mention the fast and slow steps in the mechanism:
Phenol + CHCl3 + 3 KOH -> ? (Reimer-Tiemann reaction) (5)
(ii) Identify the major product formed in the following reaction and explain the stereochemical outcome :
4-tert-butylcyclohexene + Br2 -> ? (5) upsc previous year question paper civil service combined Geo Scientist main Examination Chemistry III
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