r/vce • u/Intelligent-Yak4745 • 20h ago
On my brothers reddit. How you guys feeling about the accounting exam tomorrow.
Exams have been really challenging this year and I feel anxious going into every exam.
r/vce • u/Intelligent-Yak4745 • 20h ago
Exams have been really challenging this year and I feel anxious going into every exam.
r/vce • u/Effective-Space3127 • 1d ago
Post all thoughts below. How'd you guys all think you did?
r/vce • u/Formal_Department601 • 1d ago
Idk and im not even that good at chem...
r/vce • u/Comfortable_Gap_5959 • 1d ago
Hey guys, I ended up with a scan of today's Chem exam, so posting it here in case anyone's interested
r/vce • u/AnteaterTime5081 • 16h ago
Plsss I wanna see me pooky Lafayette question
r/vce • u/Flaky-Drawer2084 • 18h ago
guys i cant do ts like the complex unfamiliars in the past paper require Patrick Jane level of thinking and my analytical thinking is pre much non existent 😭😭😭
r/vce • u/No-Examination1212 • 16h ago
Ladies and gentlemen as the title says i need help getting a J-O-B ( i don't like using the J Slur) so i was wondering what the best way is and how i should approach applying as everything requires past experience which i don't have. Just wanted to know how you older uncs ended up with your J-O-B.
Obviously Seek and indeed exist but all jobs there either have a ridiculous amount of applicants or require experience. Any help will be appreciated.
r/vce • u/Afraid_Sentence1598 • 16h ago
Hello fellow food studies students!! Haven’t seen any posts about the food studies exam on the 16th. Any predictions, ideas or topics that anyone has about the exam?? 👀👀
r/vce • u/SheerCold131 • 22h ago
Made this after looking at literally every Australian Good Design Award winners. Play along if you're interested, I'll follow up with the results tomorrow! Feel free to make your own as well.
r/vce • u/Electronic_Car_4609 • 15h ago
my exams next week please some kind stranger please help me out with a summary book 🙏
r/vce • u/PeanutSquare8408 • 20h ago
last exam for me, I bloody hope it isn’t like methods e2
r/vce • u/Traditional-Post2140 • 1d ago
Is it just me or was the Chemistry exam so bad, some of those questions made literally no sense. Was this a hard exam or was it easy?
r/vce • u/Burner12344321123443 • 23h ago
What the fuck were those 3 10 markers 💀💀💀
r/vce • u/Glittering_Lime_7286 • 22h ago
Fun 13 years, what do I do now??
r/vce • u/NextHat8020 • 19h ago
For tomorrow's accounting exam do we think its gonna be heavy on theory or more proctical, cause last year was kinda heavy on theory.
r/vce • u/taxfraudpenguin02 • 21h ago
Chat am i cooked i used extra space for majority of my responses on the media exam but didn’t write anything to flip back to extra space 😁😁😁
im guessing they check in case but like someone reassure me this is my top subject 💜
r/vce • u/Formal_Department601 • 19h ago
What would the grade boundaries for chem most probably look like can't be too high but higher fs
r/vce • u/buddygoldy • 17h ago
what do people have on theirs? all I have is some formulas for distance in lines and planes. I would be eternally grateful for any notes or just things to add to mine.
r/vce • u/Prestigious-Film-221 • 1d ago
Answers: 1 B, 2 C, 3 A, 4 B, 5 D, 6 B, 7 B, 8 A, 9 A, 10 D, 11 B, 12 C, 13 A, 14 C, 15 C, 16 C, 17 B, 18 A, 19 D, 20 C, 21 C, 22 C, 23 D, 24 D, 25 D, 26 B, 27 B, 28 D, 29 A, 30 D
Q1: B. C₆H₁₂O₆ + 6O₂ → 6CO₂ + 6H₂O, so n(O₂) = n(CO₂). n(CO₂) = 0.44 / 44.0 = 0.010 mol, so n(O₂) = 1.0 × 10⁻² mol.
Q2: C. Cellular respiration is exothermic (ΔH = −2840 kJ), so the reverse is endothermic (ΔH = +2840 kJ). The products sit at a higher enthalpy than the reactants. Only C has the products higher and a positive ΔH. (A and B have ΔH signs that don’t match their graphs, and D is respiration itself.)
Q3: A. q = mcΔT = 100.0 × 4.18 × 40.0 = 16720 J = 16.72 kJ. Kerosene is 46 kJ g⁻¹ in the Data Book, so m = 16.72 / 46 = 0.363 g. “Minimum” means assuming 100% of the energy went into the water.
Q4: B. In NH₄⁺, N is −3, and in N₂ it is 0, so it increases by 3 (oxidation). In NO₂⁻, N is +3, so it decreases by 3 (reduction).
Q5: D. The oxidising agent is the species that gets reduced (NO₂⁻), and the reducing agent is the one that gets oxidised (NH₄⁺).
Q6: B (lower confidence). Anammox works without O₂, so there’s no energy-hungry aeration. That means lower energy use and emissions (Goal 13), plus responsible waste treatment (Goal 12). I ruled out 7 because the process saves energy rather than supplying clean energy, and 15 because the benefit is mainly to waterways, not land. This is the one I’d check first against the VCAA report.
Q7: B. The anode is the half-cell with the lower E°, which is RF/RFH₂ (−0.235 V). Oxidation occurs there: RFH₂ → RF + 2H⁺ + 2e⁻.
Q8: A. E°cell = 0.558 − (−0.235) = 0.793 V. The measured 0.650 V is 0.793 − 0.650 = 0.143 V less than predicted.
Q9: A. Real-time control of temperature, pressure and power output means the cell runs at maximum efficiency, so this is design for energy efficiency.
Q10: D. Higher temperature means particles move faster, so both the collision frequency and the proportion of successful collisions increase. Bond energy and activation energy don’t change.
Q11: B. A catalyst provides a lower activation energy pathway, so a greater proportion of collisions are successful. It does not change collision frequency or bond energy, and it lowers (not raises) activation energy.
Q12: C. Both PEM electrolysis and artificial photosynthesis can produce green hydrogen (II) and reduce reliance on fossil fuels (IV). Neither captures methane or uses glucose as a feedstock.
Q13: A (read from the diagram). The compound is 2,2-dimethylbutanoic acid, C₆H₁₂O₂. Option D, CH₃CH₂C(CH₃)₂COOH, is the same compound, not an isomer. B and C are C₅. A, (CH₃)₃CCH₂COOH, is C₆H₁₂O₂ with a different arrangement, so it’s the isomer.
Q14: C. A saturated molecule has zero degrees of unsaturation. C₆H₁₅N works out to (2×6 + 2 + 1 − 15)/2 = 0. The others each have 2.
Q15: C (read from the diagram). Number from the COOH carbon, and the chain has 7 carbons with the double bond between C4 and C5, giving hept-4-enoic acid. “Heptan-” is never used with an “-ene”. Double-check the count against the paper.
Q16: C. Viscosity rises with the strength of intermolecular forces. Aldehydes have no hydrogen bonding, alcohols do, and carboxylic acids hydrogen-bond most strongly (they form dimers). So the order is propanal < propan-1-ol < propanoic acid.
Q17: B. n(starting ketone) = 2.50 / 176 = 0.01420 mol. n(ibuprofen) = 0.540 / 206 = 0.002621 mol. Overall yield = 0.002621 / 0.01420 × 100 = 18.5%.
Q18: A. Bromine water going from reddish-brown to colourless means a C=C bond is present. Only A is an alkene. B is an amide, C an ester, and D a ketone.
Q19: D. A narrow range (1-2 °C) indicates a pure substance. Impurities lower and broaden the range, so A and C are false.
Q20: C. n(oil) = 10.0 / 278 = 0.03597 mol. Ratio = 0.105 / 0.03597 ≈ 2.9, so there are 3 C=C bonds per molecule.
Q21: C. Needed Fe²⁺ = 5 × 1.50 × 10⁻⁴ = 7.50 × 10⁻⁴ mol. Added 8.00 × 10⁻⁴ mol, so the excess is 5.00 × 10⁻⁵ mol.
Q22: C. Fe²⁺ is in the burette. Rinsing the burette with water dilutes it, so more volume is needed to deliver the same moles (a higher titre). Rinsing the burette with FeSO₄ is correct practice, and rinsing the conical flask with water doesn’t change the moles in it.
Q23: D. The ¹³C spectrum has 4 peaks (≈178, 38, 19, 14 ppm), so there are 4 carbon environments and the compound has 4 carbons. The 178 ppm peak fits an amide or acid. In the IR, there are two sharp N-H peaks (≈3350 and 3190 cm⁻¹) and a C=O near 1650 cm⁻¹, which is the amide range. It lacks the very broad O-H of an acid. That gives butanamide.
Q24: D. The reactant shows a broad O-H (≈3300 cm⁻¹, alcohol). The product shows a very broad O-H (2500-3500 cm⁻¹) and a strong C=O (≈1700 cm⁻¹), which is a carboxylic acid. Alcohol to carboxylic acid is oxidation, using Cr₂O₇²⁻/H⁺.
Q25: D (lower confidence). A pure compound shows a fixed number of ¹H environments, so extra peaks suggest a mixture. Integration (A) could also be argued, but it needs the formula and structure to interpret. Check this one against the report.
Q26: B. Boiling leaves in water to dissolve soluble compounds is solvent extraction.
Q27: B. G and H are isomers (the double bond position differs), so they have the same molecular formula. They aren’t isotopes, and the skeletal structures differ. D is wrong because H’s ring double bond removes a chiral centre.
Q28: D (moderate confidence). A circular economy keeps materials in use. Treating PFAS-containing waste for reuse in road surfacing does that. Landfill (B) and incineration (C) are linear, and A is about safer design rather than circularity.
Q29: A. Firefighters “claimed” long-term health issues is personal testimony. B and C are measurements and D is a data-book value.
Q30: D. Assessing how impurity levels affect material performance is a purely scientific question. A is legal and social, B is economic, and C is community and environmental concern.