Exponential Growth and Decay Models - Calculus 2

  1. A tank initially contains 1000 gallons of pure water. Salt water containing 2 pounds of salt per gallon flows in at 5 gallons per minute, and the well-mixed solution flows out at the same rate. The amount of salt S(t)S(t) satisfies dSdt=10−S200\frac{dS}{dt} = 10 - \frac{S}{200}. How much salt will be in the tank when the concentration reaches 1.5 pounds per gallon?
    Answer: S=1500S = 1500 pounds (concentration × volume) This is a classic mixing problem that tests your understanding of differential equations and equilibrium concepts. When you encounter these problems, focus on what the question is actually asking rather than getting caught up in solving the differential equation. The key insight is recognizing what "concentration reaches 1.5 pounds per gallon" means. Since the tank always contains 1000 gallons (inflow rate equals outflow rate), you can find the amount of salt directly: S=concentration×volume=1.5×1000=1500S = \text{concentration} \times \text{volume} = 1.5 \times 1000 = 1500 pounds. This straightforward calculation gives you the answer without needing to solve the differential equation. Let's examine why the other answers are wrong. Answer A (1200 pounds) represents 60% of the equilibrium value, which you'd get by incorrectly assuming the question asks for a percentage of maximum capacity. Answer C (1800 pounds) represents 90% of equilibrium—another percentage trap that doesn't relate to the actual concentration given. Answer D (2000 pounds) is the equilibrium value itself, which occurs when dSdt=0\frac{dS}{dt} = 0, meaning 10=S20010 = \frac{S}{200}, so S=2000S = 2000. This would correspond to the final concentration of 2 pounds per gallon, not the 1.5 pounds per gallon specified. Strategy tip: In mixing problems, always identify what the question is asking before diving into complex calculations. Often, the relationship between concentration, volume, and total amount (S=C×VS = C \times V) provides a direct path to the answer, especially when the volume remains constant.
  2. A culture of bacteria grows at a rate proportional to the number of bacteria present. The number of bacteria triples in 6 hours. By what factor will the number of bacteria increase in 18 hours?
    Answer: 27 Let P(t)P(t) be the number of bacteria. The model is P(t)=P0ektP(t) = P_0 e^{kt}. We are given that P(6)=3P0P(6) = 3P_0. So, 3P0=P0e6k3P_0 = P_0 e^{6k}, which implies e6k=3e^{6k} = 3. We want to find the factor of increase in 18 hours, which is P(18)P0\frac{P(18)}{P_0}. P(18)=P0e18k=P0e6k⋅3=P0(e6k)3P(18) = P_0 e^{18k} = P_0 e^{6k \cdot 3} = P_0 (e^{6k})^3. Since we know e6k=3e^{6k} = 3, we have P(18)=P0(3)3=27P0P(18) = P_0 (3)^3 = 27P_0. Therefore, the number of bacteria will increase by a factor of 27.
  3. Two populations, P1(t)P_1(t) and P2(t)P_2(t), grow exponentially with respective positive growth constants k1k_1 and k2k_2. Initially, at t=0t=0, the size of the first population is twice the size of the second, i.e., P1(0)=2P2(0)P_1(0) = 2P_2(0). After 5 years, the populations are equal. Which equation correctly relates the growth constants?
    Answer: k2−k1=ln⁡(2)5k_2 - k_1 = \frac{\ln(2)}{5} The population models are P1(t)=P1(0)ek1tP_1(t) = P_1(0)e^{k_1 t} and P2(t)=P2(0)ek2tP_2(t) = P_2(0)e^{k_2 t}. Let P2(0)=AP_2(0) = A, so P1(0)=2AP_1(0) = 2A. At t=5t=5, we have P1(5)=P2(5)P_1(5) = P_2(5). Substituting the models gives (2A)e5k1=(A)e5k2(2A)e^{5k_1} = (A)e^{5k_2}. Dividing by AA (since A>0A>0) gives 2e5k1=e5k22e^{5k_1} = e^{5k_2}. Taking the natural logarithm of both sides gives ln⁡(2e5k1)=ln⁡(e5k2)\ln(2e^{5k_1}) = \ln(e^{5k_2}), which simplifies to ln⁡(2)+5k1=5k2\ln(2) + 5k_1 = 5k_2. Rearranging the terms to relate k1k_1 and k2k_2 gives 5k2−5k1=ln⁡(2)5k_2 - 5k_1 = \ln(2), or k2−k1=ln⁡(2)5k_2 - k_1 = \frac{\ln(2)}{5}.
  4. A quantity y(t)y(t) follows the law of exponential decay, dydt=−ky\frac{dy}{dt} = -ky for a constant k>0k>0. Which of the following linear, homogeneous, second-order differential equations with constant coefficients is also satisfied by y(t)y(t)?
    Answer: d2ydt2+kdydt=0\frac{d^2y}{dt^2} + k \frac{dy}{dt} = 0 Given dydt=−ky\frac{dy}{dt} = -ky. We can differentiate this equation with respect to tt to find a second-order equation: ddt(dydt)=ddt(−ky)\frac{d}{dt}\left(\frac{dy}{dt}\right) = \frac{d}{dt}(-ky), which gives d2ydt2=−kdydt\frac{d^2y}{dt^2} = -k \frac{dy}{dt}. Rearranging gives d2ydt2+kdydt=0\frac{d^2y}{dt^2} + k \frac{dy}{dt} = 0. This is a linear, homogeneous, second-order differential equation with constant coefficients. Choices A and C have incorrect forms, and choice D has the wrong sign.
  5. The rate of change of a quantity yy is directly proportional to yy. It is known that at time t1t_1, the value of the quantity is aa, and at time t2t_2, its value is bb. What is the value of the quantity at time 2t2−t12t_2 - t_1?
    Answer: b2a\frac{b^2}{a} The governing equation is dydt=ky\frac{dy}{dt} = ky, so y(t)=y0ekty(t) = y_0 e^{kt}. We are given y(t1)=a=y0ekt1y(t_1) = a = y_0 e^{kt_1} and y(t2)=b=y0ekt2y(t_2) = b = y_0 e^{kt_2}. Dividing these gives ba=y0ekt2y0ekt1=ek(t2−t1)\frac{b}{a} = \frac{y_0 e^{kt_2}}{y_0 e^{kt_1}} = e^{k(t_2 - t_1)}. We want to find y(2t2−t1)=y0ek(2t2−t1)y(2t_2 - t_1) = y_0 e^{k(2t_2 - t_1)}. We can rewrite the exponent as k(t2+(t2−t1))k(t_2 + (t_2 - t_1)). So, y(2t2−t1)=y0ekt2ek(t2−t1)y(2t_2-t_1) = y_0 e^{kt_2} e^{k(t_2 - t_1)}. We know y0ekt2=y(t2)=by_0 e^{kt_2} = y(t_2) = b and ek(t2−t1)=bae^{k(t_2 - t_1)} = \frac{b}{a}. Therefore, y(2t2−t1)=b⋅ba=b2ay(2t_2 - t_1) = b \cdot \frac{b}{a} = \frac{b^2}{a}.
  6. Newton's Law of Cooling states that dTdt=−k(T−Tamb)\frac{dT}{dt} = -k(T - T_{amb}), where TT is temperature, TambT_{amb} is ambient temperature, and k>0k > 0. A cup of coffee at 90°C is placed in a 20°C room. After 10 minutes, the temperature is 70°C. What will the temperature be after 20 minutes?
    Answer: T(20)=20+50⋅(57)2=20+125049≈45.5°CT(20) = 20 + 50 \cdot (\frac{5}{7})^2 = 20 + \frac{1250}{49} \approx 45.5°C Newton's Law of Cooling problems require solving a separable differential equation. When you see dTdt=−k(T−Tamb)\frac{dT}{dt} = -k(T - T_{amb}), recognize this as exponential decay toward the ambient temperature. Start by separating variables and integrating: dTT−Tamb=−k dt\frac{dT}{T - T_{amb}} = -k \, dt. This gives us T(t)=Tamb+(T0−Tamb)e−ktT(t) = T_{amb} + (T_0 - T_{amb})e^{-kt}, where T0T_0 is the initial temperature. With Tamb=20°CT_{amb} = 20°C and T0=90°CT_0 = 90°C, we have T(t)=20+70e−ktT(t) = 20 + 70e^{-kt}. Using the condition that T(10)=70°CT(10) = 70°C: 70=20+70e−10k70 = 20 + 70e^{-10k} 50=70e−10k50 = 70e^{-10k} e−10k=57e^{-10k} = \frac{5}{7} For t=20t = 20 minutes: T(20)=20+70e−20k=20+70(e−10k)2=20+70(57)2=20+70⋅2549=20+125049≈45.5°CT(20) = 20 + 70e^{-20k} = 20 + 70(e^{-10k})^2 = 20 + 70(\frac{5}{7})^2 = 20 + 70 \cdot \frac{25}{49} = 20 + \frac{1250}{49} \approx 45.5°C. This matches answer C. Answer A incorrectly uses 70⋅e−2k⋅1070 \cdot e^{-2k \cdot 10} instead of the proper exponential form with the calculated decay constant. Answer B assumes linear cooling, but Newton's Law describes exponential decay, not linear change. Answer D uses the correct exponential structure but incorrectly substitutes 5070\frac{50}{70} directly for e−10ke^{-10k}, missing that we need e−10k=57e^{-10k} = \frac{5}{7}. Study tip: Always find the decay constant using given conditions before plugging in your target time. Don't assume linear relationships in exponential decay problems.
  7. A cup of coffee at 90°C is placed in a room. After 10 minutes, its temperature is 70°C. After another 10 minutes, its temperature is 55°C. Assuming the coffee cools according to Newton's Law of Cooling, what is the ambient temperature of the room?
    Answer: 10°C Let T(t)T(t) be the temperature and TsT_s be the room temperature. Newton's Law of Cooling is dTdt=k(T−Ts)\frac{dT}{dt} = k(T - T_s), with solution T(t)=Ts+(T0−Ts)ektT(t) = T_s + (T_0 - T_s)e^{kt}. We have T(0)=90T(0)=90, T(10)=70T(10)=70, and T(20)=55T(20)=55. From these, we get the equations: 70=Ts+(90−Ts)e10k70 = T_s + (90-T_s)e^{10k} and 55=Ts+(90−Ts)e20k55 = T_s + (90-T_s)e^{20k}. Let x=e10kx = e^{10k}. The equations become 70−Ts=(90−Ts)x70 - T_s = (90-T_s)x and 55−Ts=(90−Ts)x255 - T_s = (90-T_s)x^2. From the first equation, x=70−Ts90−Tsx = \frac{70-T_s}{90-T_s}. Substituting this into the second equation gives 55−Ts=(90−Ts)(70−Ts90−Ts)255 - T_s = (90 - T_s) \left(\frac{70-T_s}{90-T_s}\right)^2, which simplifies to (55−Ts)(90−Ts)=(70−Ts)2(55-T_s)(90-T_s) = (70-T_s)^2. Expanding both sides yields 4950−145Ts+Ts2=4900−140Ts+Ts24950 - 145T_s + T_s^2 = 4900 - 140T_s + T_s^2. Solving for TsT_s gives 50=5Ts50 = 5T_s, so Ts=10T_s = 10.
  8. An object is cooling in an environment with an ambient temperature of 20°C. At 2:00 PM, its temperature is 60°C. At 3:00 PM, its temperature is 40°C. What was the object's temperature at 1:00 PM?
    Answer: 100°C When you encounter a cooling problem like this, you're dealing with Newton's Law of Cooling, which states that temperature follows an exponential decay model: T(t)=Tambient+(T0−Tambient)e−ktT(t) = T_{\text{ambient}} + (T_0 - T_{\text{ambient}})e^{-kt} Let's set up the problem systematically. The ambient temperature is 20°C, so our equation becomes T(t)=20+(T0−20)e−ktT(t) = 20 + (T_0 - 20)e^{-kt}, where T0T_0 is the initial temperature and kk is the cooling constant. Using the given data points: at t=1t = 1 hour (3:00 PM), T=40°CT = 40°C, and at t=0t = 0 (2:00 PM), T=60°CT = 60°C. From the 2:00 PM data: 60=20+(T0−20)e060 = 20 + (T_0 - 20)e^0, which gives us T0−20=40T_0 - 20 = 40. From the 3:00 PM data: 40=20+40e−k40 = 20 + 40e^{-k}, so e−k=0.5e^{-k} = 0.5. To find the temperature at 1:00 PM (t=−1t = -1), we need ek=2e^{k} = 2. Therefore: T(−1)=20+40ek=20+40(2)=100°CT(-1) = 20 + 40e^{k} = 20 + 40(2) = 100°C. Choice A (80°C) assumes linear cooling rather than exponential. Choice B (90°C) might come from averaging incorrectly. Choice C (120°C) results from doubling the temperature difference without accounting for the exponential nature. The correct answer is D (100°C). Remember: cooling problems always involve exponential decay, not linear relationships. When temperatures are given at regular intervals, use the exponential pattern to work backward or forward in time.
  9. A 100-liter tank initially contains pure water. A salt solution with a concentration of 0.5 kg/L is added at a rate of 4 L/min. The solution is kept thoroughly mixed and drains from the tank at the same rate of 4 L/min. How many minutes does it take for the concentration of salt in the tank to reach 0.25 kg/L?
    Answer: 25ln⁡(2)25 \ln(2) Let A(t)A(t) be the amount of salt in kg. The volume is constant at V=100V=100 L. The rate of change is dAdt=(rate in)−(rate out)\frac{dA}{dt} = (\text{rate in}) - (\text{rate out}). Rate in = (0.5 kg/L)×(4 L/min)=2(0.5 \text{ kg/L}) \times (4 \text{ L/min}) = 2 kg/min. Rate out = (A(t)100 kg/L)×(4 L/min)=A25(\frac{A(t)}{100} \text{ kg/L}) \times (4 \text{ L/min}) = \frac{A}{25}. The DE is dAdt=2−A25\frac{dA}{dt} = 2 - \frac{A}{25}. The solution to this linear DE with A(0)=0A(0)=0 is A(t)=50(1−e−t/25)A(t) = 50(1 - e^{-t/25}). We want the time tt when the concentration is 0.25 kg/L, which means A(t)=0.25×100=25A(t) = 0.25 \times 100 = 25 kg. So, 25=50(1−e−t/25)⇒0.5=1−e−t/25⇒e−t/25=0.525 = 50(1 - e^{-t/25}) \Rightarrow 0.5 = 1 - e^{-t/25} \Rightarrow e^{-t/25} = 0.5. Taking the natural log, −t/25=ln⁡(0.5)=−ln⁡(2)-t/25 = \ln(0.5) = -\ln(2). Thus, t=25ln⁡(2)t = 25 \ln(2).
  10. The value of a machine, V(t)V(t) in dollars, depreciates according to the differential equation dVdt=−0.15V\frac{dV}{dt} = -0.15V, where tt is in years. The initial value is V(0)=$20,000V(0) = \$20,000. What is the correct interpretation of the quantity 15∫05V(t)dt\frac{1}{5}\int_0^5 V(t) dt?
    Answer: The average value of the machine over the first 5 years. The expression 1b−a∫abf(x)dx\frac{1}{b-a}\int_a^b f(x) dx is the definition of the average value of a function f(x)f(x) on the interval [a,b][a, b]. In this context, with V(t)V(t) representing the value of the machine at time tt, the expression 15−0∫05V(t)dt\frac{1}{5-0}\int_0^5 V(t) dt represents the average value of the machine over the time interval from t=0t=0 to t=5t=5 years. The other choices represent different quantities: total depreciation is V(0)−V(5)V(0)-V(5), instantaneous rate is V′(5)V'(5), and value at 5 years is V(5)V(5).
  11. A bank account with continuous compounding at an annual rate rr is modeled by dBdt=rB\frac{dB}{dt} = rB. If an initial deposit of PP quadruples in 18 years, in how many years will the initial deposit triple?
    Answer: 18ln⁡(3)ln⁡(4)18 \frac{\ln(3)}{\ln(4)} years When you encounter differential equations modeling exponential growth like dBdt=rB\frac{dB}{dt} = rB, you're dealing with continuous compounding problems that follow the pattern B(t)=PertB(t) = Pe^{rt}. The key insight is using given information to find relationships between different time scenarios. Since the account quadruples in 18 years, we have 4P=Pe18r4P = Pe^{18r}, which simplifies to 4=e18r4 = e^{18r}. Taking the natural logarithm: ln⁡(4)=18r\ln(4) = 18r, so r=ln⁡(4)18r = \frac{\ln(4)}{18}. Now we need to find when the account triples: 3P=Pert3P = Pe^{rt}, giving us 3=ert3 = e^{rt}. Taking the natural logarithm: ln⁡(3)=rt=t⋅ln⁡(4)18\ln(3) = rt = t \cdot \frac{\ln(4)}{18}. Solving for t: t=18ln⁡(3)ln⁡(4)t = \frac{18\ln(3)}{\ln(4)}. Looking at the wrong answers: Choice A (9 years) incorrectly assumes tripling takes half the time of quadrupling, which only works for linear growth, not exponential. Choice B (12 years) might come from incorrectly thinking tripling takes 34\frac{3}{4} the time of quadrupling (18×34=13.518 \times \frac{3}{4} = 13.5, rounded to 12). Choice C has the logarithms inverted—this would give the wrong relationship between the growth rates. The correct answer is D: 18ln⁡(3)ln⁡(4)18 \frac{\ln(3)}{\ln(4)} years. Study tip: In exponential growth problems, always use the given condition to find the growth rate first, then apply it to the desired scenario. Remember that time ratios in exponential growth involve logarithms, not simple proportions.
  12. An account balance B(t)B(t) earns interest at a rate proportional to the current balance, with an annual proportionality constant rr. Simultaneously, continuous withdrawals are made at a rate proportional to the square root of the balance, with a proportionality constant ww. Which differential equation correctly models the balance B(t)B(t) over time?
    Answer: dBdt=rB−wB\frac{dB}{dt} = rB - w\sqrt{B} The differential equation is built by considering the rates of increase and decrease of the balance. The phrase 'earns interest at a rate proportional to the current balance' translates to an interest rate term of +rB+rB. The phrase 'continuous withdrawals are made at a rate proportional to the square root of the balance' translates to a withdrawal term of −wB-w\sqrt{B}. Combining these two terms gives the net rate of change of the balance: dBdt=rB−wB\frac{dB}{dt} = rB - w\sqrt{B}.
  13. The rate of formation of a chemical product is proportional to the amount of unreacted substrate remaining. Initially, there are 100 grams of substrate. After 1 hour, 50 grams remain. What is the amount of substrate remaining after a total of 3 hours?
    Answer: 12.5 grams Let S(t)S(t) be the amount of substrate remaining. The problem states dSdt=−kS\frac{dS}{dt} = -kS for some k>0k>0. We are given S(0)=100S(0) = 100 and S(1)=50S(1) = 50. Since the amount was reduced by half in 1 hour, the half-life is 1 hour. The amount of substrate remaining after tt hours is given by S(t)=100(1/2)t/1=100(1/2)tS(t) = 100 (1/2)^{t/1} = 100 (1/2)^t. We want to find the amount remaining after 3 hours, which is S(3)=100(1/2)3=100(1/8)=12.5S(3) = 100 (1/2)^3 = 100 (1/8) = 12.5 grams.
  14. A 1000-liter tank initially contains 500 liters of brine with 50 kg of dissolved salt. Brine containing 0.2 kg of salt per liter is pumped into the tank at a rate of 10 L/min. The well-mixed solution is pumped out at a rate of 5 L/min. Which differential equation models the amount of salt A(t)A(t) in kilograms in the tank at time tt in minutes?
    Answer: dAdt=2−A100+t\frac{dA}{dt} = 2 - \frac{A}{100+t} The rate of change of salt is dAdt=(rate in)−(rate out)\frac{dA}{dt} = (\text{rate in}) - (\text{rate out}). The rate of salt flowing in is (0.2 kg/L)×(10 L/min)=2 kg/min(0.2 \text{ kg/L}) \times (10 \text{ L/min}) = 2 \text{ kg/min}. The volume of the solution in the tank changes over time. Initially V(0)=500V(0)=500 L. Since liquid flows in at 10 L/min and out at 5 L/min, the net change is +5 L/min. So, V(t)=500+5tV(t) = 500 + 5t. The concentration of salt at time tt is C(t)=A(t)V(t)=A(t)500+5tC(t) = \frac{A(t)}{V(t)} = \frac{A(t)}{500+5t} kg/L. The rate of salt flowing out is C(t)×(outflow rate)=A(t)500+5t×5=5A(t)500+5t=A(t)100+tC(t) \times (\text{outflow rate}) = \frac{A(t)}{500+5t} \times 5 = \frac{5A(t)}{500+5t} = \frac{A(t)}{100+t}. Combining these gives dAdt=2−A100+t\frac{dA}{dt} = 2 - \frac{A}{100+t}.
  15. Carbon-14 dating is used to determine the age of an ancient artifact. The decay model is dCdt=−λC\frac{dC}{dt} = -\lambda C with half-life 5730 years. If the artifact currently contains 25% of the original carbon-14, approximately how old is the artifact?
    Answer: 11,460 years (exactly 2 half-lives) If 25% remains, then 75% has decayed. Since C(t)=C0e−λtC(t) = C_0 e^{-\lambda t}, we have 0.25C0=C0e−λt0.25C_0 = C_0 e^{-\lambda t}, so 0.25=e−λt0.25 = e^{-\lambda t}. Taking ln: ln⁡(0.25)=−λt\ln(0.25) = -\lambda t, giving t=ln⁡(4)λt = \frac{\ln(4)}{\lambda}. Since λ=ln⁡(2)5730\lambda = \frac{\ln(2)}{5730}, we get t=ln⁡(4)⋅5730ln⁡(2)=2ln⁡(2)⋅5730ln⁡(2)=11,460t = \frac{\ln(4) \cdot 5730}{\ln(2)} = \frac{2\ln(2) \cdot 5730}{\ln(2)} = 11,460 years. This is exactly 2 half-lives since (1/2)2=1/4=0.25(1/2)^2 = 1/4 = 0.25. Choice B uses the correct formula but miscalculates. Choice C assumes 2.5 half-lives. Choice D assumes 4 half-lives.
  16. A hot object is placed in a room with a constant ambient temperature. According to Newton's Law of Cooling, the temperature difference between the object and the room decreases by 50% in the first 10 minutes. By what percentage does this temperature difference decrease over the first 20 minutes?
    Answer: 75% Let D(t)=T(t)−TsD(t) = T(t) - T_s be the temperature difference. It follows the model dDdt=kD\frac{dD}{dt} = kD, with solution D(t)=D0ektD(t) = D_0 e^{kt}. A 50% decrease in 10 minutes means D(10)=0.5D0D(10) = 0.5 D_0. This is the definition of half-life, so the half-life of the temperature difference is 10 minutes. After another 10 minutes (for a total of 20 minutes), another half-life has passed. The difference will be halved again: D(20)=0.5D(10)=0.5(0.5D0)=0.25D0D(20) = 0.5 D(10) = 0.5(0.5 D_0) = 0.25 D_0. If 25% of the difference remains, the total decrease is 100100% - 25% = 75%.
  17. A chemical reaction follows first-order kinetics: d[A]dt=−k[A]\frac{d[A]}{dt} = -k[A], where [A][A] is the concentration of reactant A. If the reaction is 80% complete after 45 minutes, what is the half-life of the reaction?
    Answer: t1/2=45ln⁡(2)ln⁡(5)≈19.4t_{1/2} = \frac{45\ln(2)}{\ln(5)} \approx 19.4 minutes When you encounter first-order kinetics problems, you're dealing with exponential decay where the rate of change is proportional to the current amount. The key is solving the differential equation and connecting different time points. Starting with d[A]dt=−k[A]\frac{d[A]}{dt} = -k[A], separation of variables gives us d[A][A]=−k dt\frac{d[A]}{[A]} = -k \, dt. Integrating both sides yields ln⁡[A]=−kt+C\ln[A] = -kt + C, or [A]=[A]0e−kt[A] = [A]_0 e^{-kt} where [A]0[A]_0 is the initial concentration. If the reaction is 80% complete after 45 minutes, then 20% of the original reactant remains: [A]=0.2[A]0[A] = 0.2[A]_0. Substituting into our equation: 0.2[A]0=[A]0e−45k0.2[A]_0 = [A]_0 e^{-45k}, which simplifies to 0.2=e−45k0.2 = e^{-45k}. Taking the natural logarithm: ln⁡(0.2)=−45k\ln(0.2) = -45k, so k=−ln⁡(0.2)45=ln⁡(5)45k = -\frac{\ln(0.2)}{45} = \frac{\ln(5)}{45}. For half-life, we need the time when [A]=0.5[A]0[A] = 0.5[A]_0: 0.5=e−kt1/20.5 = e^{-kt_{1/2}}. This gives us ln⁡(0.5)=−kt1/2\ln(0.5) = -kt_{1/2}, so t1/2=ln⁡(2)k=45ln⁡(2)ln⁡(5)t_{1/2} = \frac{\ln(2)}{k} = \frac{45\ln(2)}{\ln(5)}, which is answer D. A incorrectly multiplies by ln⁡(2)\ln(2) instead of dividing by the rate constant. B naively assumes linear decay rather than exponential. C uses ln⁡(0.2)\ln(0.2) in the denominator but forgets that ln⁡(0.2)=−ln⁡(5)\ln(0.2) = -\ln(5), missing the sign change. Remember: for first-order kinetics, always solve for the rate constant first using given information, then apply it to find other time-related quantities.
  18. The population P(t)P(t) of a certain species grows in such a way that the rate of change of its relative growth rate is proportional to the current population. The relative growth rate is defined as 1PdPdt\frac{1}{P}\frac{dP}{dt}. Which differential equation correctly models this scenario, where cc is a constant of proportionality?
    Answer: ddt(1PdPdt)=cP\frac{d}{dt}\left( \frac{1}{P}\frac{dP}{dt} \right) = cP Let's translate the statement piece by piece. The 'relative growth rate' is given as R=1PdPdtR = \frac{1}{P}\frac{dP}{dt}. The 'rate of change of its relative growth rate' is the derivative of RR with respect to time, dRdt=ddt(1PdPdt)\frac{dR}{dt} = \frac{d}{dt}\left( \frac{1}{P}\frac{dP}{dt} \right). The statement says this quantity is 'proportional to the current population', which means it equals cPcP for some constant cc. Therefore, the correct differential equation is ddt(1PdPdt)=cP\frac{d}{dt}\left( \frac{1}{P}\frac{dP}{dt} \right) = cP.
  19. A quantity yy grows exponentially according to y(t)=y0ekty(t) = y_0 e^{kt}. It is observed that the quantity doubles from its initial value at time t=Tt=T, and it triples from its initial value at time t=T+5t=T+5. What is the value of the doubling time TT?
    Answer: 5ln⁡(2)ln⁡(3)−ln⁡(2)5 \frac{\ln(2)}{\ln(3) - \ln(2)} We are given two conditions: y(T)=2y0y(T) = 2y_0 and y(T+5)=3y0y(T+5) = 3y_0. Using the solution form, these become y0ekT=2y0y_0 e^{kT} = 2y_0 and y0ek(T+5)=3y0y_0 e^{k(T+5)} = 3y_0. The first equation simplifies to ekT=2e^{kT} = 2. The second becomes ekTe5k=3e^{kT}e^{5k} = 3. Substituting ekT=2e^{kT}=2 into the second simplified equation gives 2e5k=32e^{5k} = 3, so e5k=1.5e^{5k} = 1.5. From ekT=2e^{kT}=2, we have kT=ln⁡(2)kT = \ln(2), so k=ln⁡(2)Tk = \frac{\ln(2)}{T}. From e5k=1.5e^{5k} = 1.5, we have 5k=ln⁡(1.5)5k = \ln(1.5), so k=ln⁡(1.5)5k = \frac{\ln(1.5)}{5}. Equating the two expressions for kk gives ln⁡(2)T=ln⁡(1.5)5\frac{\ln(2)}{T} = \frac{\ln(1.5)}{5}. Solving for TT yields T=5ln⁡(2)ln⁡(1.5)=5ln⁡(2)ln⁡(3/2)=5ln⁡(2)ln⁡(3)−ln⁡(2)T = 5 \frac{\ln(2)}{\ln(1.5)} = 5 \frac{\ln(2)}{\ln(3/2)} = 5 \frac{\ln(2)}{\ln(3) - \ln(2)}.
  20. The concentration of a drug in the bloodstream, C(t)C(t), decays exponentially after an injection. The initial concentration is 1.2 mg/L. After 4 hours, the concentration is 0.3 mg/L. To be effective, the concentration must be at least 0.1 mg/L. For how many total hours after the injection is the drug effective?
    Answer: 4+2log⁡2(3)4 + 2\log_2(3) The model is C(t)=C0ektC(t) = C_0 e^{kt} with C0=1.2C_0 = 1.2. We are given C(4)=0.3C(4) = 0.3. So, 0.3=1.2e4k0.3 = 1.2 e^{4k}, which gives e4k=0.3/1.2=1/4e^{4k} = 0.3/1.2 = 1/4. Taking the natural log, 4k=ln⁡(1/4)=−2ln⁡(2)4k = \ln(1/4) = -2\ln(2), so k=−ln⁡(2)2k = -\frac{\ln(2)}{2}. This implies a half-life of 2 hours. We need to find the time tt for which C(t)=0.1C(t) = 0.1. So, 0.1=1.2ekt0.1 = 1.2 e^{kt}, which gives ekt=0.11.2=112e^{kt} = \frac{0.1}{1.2} = \frac{1}{12}. Taking the log, kt=ln⁡(1/12)=−ln⁡(12)kt = \ln(1/12) = -\ln(12). Substituting for kk, (−ln⁡(2)2)t=−ln⁡(12)(-\frac{\ln(2)}{2})t = -\ln(12). Solving for tt gives t=2ln⁡(12)ln⁡(2)=2log⁡2(12)t = \frac{2\ln(12)}{\ln(2)} = 2\log_2(12). We can simplify this: t=2log⁡2(4⋅3)=2(log⁡2(4)+log⁡2(3))=2(2+log⁡2(3))=4+2log⁡2(3)t = 2\log_2(4 \cdot 3) = 2(\log_2(4) + \log_2(3)) = 2(2 + \log_2(3)) = 4 + 2\log_2(3).

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