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The correct answers are : a, b, f, g.
![e> 2-bromo bicyelo (..o] butane . Achiral • Br -Br Structure o-plane presents +> 2-Huoro bicyclo (2.2.2]octane : Chiral Chira](http://img.homeworklib.com/questions/d472f070-d703-11ea-8bfc-b5bab19c8cf3.png?x-oss-process=image/resize,w_560)
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5.33 Which of the following are chiral and, therefore, capable of...
b. Which of the following alkanes has the highest bolling point? 2,3-dimethylbutane: 2-methylpentane; 3-methylpentane; hexane c....
b. Which of the following alkanes has the highest bolling point? 2,3-dimethylbutane: 2-methylpentane; 3-methylpentane; hexane c. Which of the following compounds can adopt a chair conformation in which there are no axial methyl groups? 1,1-dimethylcyclohexane; cis-1,2-dimethylcyclohexane; trans-1,2-dimethylcyclohexane; trans-1,3-di methylcyclohexane d. Which of the following compounds can adopt a chair conformation which there are no axial methyl groups? cis-1,2-dimethylcyclohexane; cis-1,3-dimethylcyclohexane; trans-1,3-dimethylcyclohexane; cis-1.4-dimethylcyclohexane cis-1,2-dimethvcyclohexane (Enter the numerical value only, without any units)? e. What is the approximate di hedral angle between the...
please show all steps and explain thoroughly ! thank you! 2. An individual is heterozygous for...
please show all steps and explain thoroughly ! thank
you!
2. An individual is heterozygous for an inversion chromosome as shown below: Q R S T E F G H Q R S 9 3 1 H A. Draw the looped arrangement of the chromosomes that you would expect to see when they are paired for meiosis I. (Although there are four strands present at meiosis I, only two are shown here; you need only draw two strands). B. Assume...
please explain and show steps V. 15.102. Predict which solution in each pair below will have...
please explain and show steps
V. 15.102. Predict which solution in each pair below will have the b. 1.00 X 10" M acetic acid (K = 1.76 X 10-5) or a. 2.56 102 M HCl or 4.09 x 10-2 MHBr lower pH. 1.00 x 10-5 M formic acid (K4 = 1.77 x 10-4) c. 22 mM CH3NH2 (pK6 = 3.36) or 22 mM(CH3)2NH (Kb = 5.9 x 10-4) d. 158 mM NH3 (pKo = 4.75) or 158 mM acetic acid...
Please explain and show steps! Thanks! At 35°C, K = 1.6×10-5 for the following reaction 2...
Please explain and show steps! Thanks!
At 35°C, K = 1.6×10-5 for the following reaction 2 NOCI(g)2 NO(g) + Cl2(g) Calculate the concentrations of all species at equilibrium for each of the following original mixtures (a) 2.0 mol of pure NOCl in a 1.7-L flask [NOCI] [Cl2l (b) 7.2 mol of NO and 3.6 mol of Cl2 in a 1.2-L flask [NOCI] [NO] [Cl2l (c) 1.7 mol of NOCI and 1.7 mol of NO in a 2.0-L flask [NOCI] [NO]...
Could you please show all of the steps taken in solving the problem and explain the process fully...
Could you please show all of the steps taken in solving the
problem and explain the process fully, using sentences/phrases (if
possible) to understand why those steps were taken and
why you got that answer.
Also could you please draw a diagram with any applicable
variables/values to help visualize the problem better.
Thank you in advance for all the help!
A 1.20-cm-tall object is 50.0 cm to the left of a diverging lens (lens 1) of focal length of magnitude...
Please complete for Tuesday, we will go through the questions and mark them in class. pg 156 - 4.23,...
Please complete for Tuesday, we will go through the questions and mark them in class. pg 156 - 4.23, 4.24, 4.26 pg 170 - 4.29, 4.31, pg 171-4.36 pg 175 - 4.59 pg 176- 4.74, 4.75, 4.80 pg 177-4.81, 4.82 pg 188- 5.1, 5.4, 5.5, 5.6, 5.11 - Using Table 5.1 pg 198-5.22, 5.25 pg 203 - 5.29 pg 206 - 5.37 pg 209 - 5.39 pg 2.14 5.61 pg 235-6.11, 6.14, 6.16 156 CHAPTER 4 Introduction to Organic Compounds...
b. Which of the following alkanes has the highest bolling point? 2,3-dimethylbutane: 2-methylpentane; 3-methylpentane; hexane c. Which of the following compounds can adopt a chair conformation in which there are no axial methyl groups? 1,1-dimethylcyclohexane; cis-1,2-dimethylcyclohexane; trans-1,2-dimethylcyclohexane; trans-1,3-di methylcyclohexane d. Which of the following compounds can adopt a chair conformation which there are no axial methyl groups? cis-1,2-dimethylcyclohexane; cis-1,3-dimethylcyclohexane; trans-1,3-dimethylcyclohexane; cis-1.4-dimethylcyclohexane cis-1,2-dimethvcyclohexane (Enter the numerical value only, without any units)? e. What is the approximate di hedral angle between the...
please show all steps and explain thoroughly ! thank
you!
2. An individual is heterozygous for an inversion chromosome as shown below: Q R S T E F G H Q R S 9 3 1 H A. Draw the looped arrangement of the chromosomes that you would expect to see when they are paired for meiosis I. (Although there are four strands present at meiosis I, only two are shown here; you need only draw two strands). B. Assume...
please explain and show steps
V. 15.102. Predict which solution in each pair below will have the b. 1.00 X 10" M acetic acid (K = 1.76 X 10-5) or a. 2.56 102 M HCl or 4.09 x 10-2 MHBr lower pH. 1.00 x 10-5 M formic acid (K4 = 1.77 x 10-4) c. 22 mM CH3NH2 (pK6 = 3.36) or 22 mM(CH3)2NH (Kb = 5.9 x 10-4) d. 158 mM NH3 (pKo = 4.75) or 158 mM acetic acid...
Please explain and show steps! Thanks!
At 35°C, K = 1.6×10-5 for the following reaction 2 NOCI(g)2 NO(g) + Cl2(g) Calculate the concentrations of all species at equilibrium for each of the following original mixtures (a) 2.0 mol of pure NOCl in a 1.7-L flask [NOCI] [Cl2l (b) 7.2 mol of NO and 3.6 mol of Cl2 in a 1.2-L flask [NOCI] [NO] [Cl2l (c) 1.7 mol of NOCI and 1.7 mol of NO in a 2.0-L flask [NOCI] [NO]...
Could you please show all of the steps taken in solving the
problem and explain the process fully, using sentences/phrases (if
possible) to understand why those steps were taken and
why you got that answer.
Also could you please draw a diagram with any applicable
variables/values to help visualize the problem better.
Thank you in advance for all the help!
A 1.20-cm-tall object is 50.0 cm to the left of a diverging lens (lens 1) of focal length of magnitude...
Please complete for Tuesday, we will go through the questions and mark them in class. pg 156 - 4.23, 4.24, 4.26 pg 170 - 4.29, 4.31, pg 171-4.36 pg 175 - 4.59 pg 176- 4.74, 4.75, 4.80 pg 177-4.81, 4.82 pg 188- 5.1, 5.4, 5.5, 5.6, 5.11 - Using Table 5.1 pg 198-5.22, 5.25 pg 203 - 5.29 pg 206 - 5.37 pg 209 - 5.39 pg 2.14 5.61 pg 235-6.11, 6.14, 6.16 156 CHAPTER 4 Introduction to Organic Compounds...
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