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please explain why Later in the course, we will compare the halogenation of differently substituted carbons, compari...
please answer all parts, thanks! 1. More substituted alkenes are more stable than less substituted alkenes....
please answer all parts, thanks!
1. More substituted alkenes are more stable than less substituted alkenes. Show the orbital overlap that helps to explain this observation. 2. Why is the heat of hydrogenation for an alkene exothermic? Analyze the bonds that are changing. AH = -30 kcal/mol Explain: + H2 3. Treating alkene "A" below with HBr can lead to a number of products. "A" SM + H-Br A bunch of products. For real, hella products. 3.A. Label the stereocenters...
pleas help 5,6,7,8,9,10 III IV 5. The product of free-radical halogenation reactions is an alkyl halide....
pleas help 5,6,7,8,9,10
III IV 5. The product of free-radical halogenation reactions is an alkyl halide. The major amount of this halide forms during the second step of propagation. However, you should be aware that one possible termination step also forms alkyl halides. Why does the majority of the alkyl halide product come from the propagation step and not the termination step? A. At any given time during the reaction, the concentration of both the alkyl radical and the halide...
EXPLAIN IN DETAIL , PLEASE( LIKE WHERE DO U GET THAT FROM? OR WHY DO WE...
EXPLAIN IN DETAIL , PLEASE(
LIKE WHERE DO U GET THAT FROM? OR WHY DO WE HAVE TO DO THAT?)
15. Given the enthalpy changes for the following reactions... Equation 1 6MnO(s) + O2(g) → 2 MnO4(s) Equation 2 2Mn2O3(s) + O2(g) → 4MnO2(s) AH° = -464kJ AH° = -142 kJ AH° = -136 kJ Equations 3 Mno(s) + 1/2O2(g) → MnO2(s) It is possible to determine the enthalpy change for the reaction below: "Final Equation" 4Mn304(s) + O2(g) →...
the answers i circled are incorrect except for 19. can you please tell me why this...
the answers i circled are incorrect except for 19. can you
please tell me why this is correct. can you give me the correct
answers and explain why?
actions usually proceed with amounts of inversion and retention at the center undergoing sustitution more inversion than retention at the center undergoing substitution y more retention then in version at the center undergoing substitution lete inversion at the center undergoing sostituti plete retention at the center undergoing substitution Which of the following...
can you please explain why did he chose the circled product as a major ? I only need explaination for part a please...
can you please explain why did he chose the circled product as
a major ?
I only need explaination for part a please
explaination for part A for both questions please
For the following a) Circle the major organic product (1 pt) reaction: b) Provide a mechanism for the initiation and two propagation steps (major only) (5 pts) c) Calculate AH001. AH , and AH (4 pts) d) Which is the rate determining propagation step (1 pt)? Explain (3 pts)...
help please. be as specific as possibly please -sincerley student in need all of the information...
help please. be as specific as possibly please
-sincerley student in need
all
of the information needed is in the image
Model 7: Which H Will Be Replaced by X? In a radical halogenation reaction a halogen (F, CI, Br or I) replaces an H. In most cases there is more than one type of H to choose from. For example the hydrocarbon below has two different types of H's: CH3 сн CHs hy CH or CH Н-С н,с CH3...
Font Open the Le Chatler's Principle Activity found in your textbook, Interactive General Chemistry. (Section 15.6,...
Font Open the Le Chatler's Principle Activity found in your textbook, Interactive General Chemistry. (Section 15.6, Figure 15.9), run the simulation and complete the following questions. 1. Start with the default settings where K = 1.00. a. Write the expression based on the chemical equation in the upper right corner. b. Under the initial conditions of (A) = 2.00 M, and (B) = 4.00 M, is the reaction at equilibrium? How can you tell? c. Compare how Q is affected...
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...
= 1-Lab from Chapter 15 Eq and Le Chat - Word Search Design Layout References Mailings...
= 1-Lab from Chapter 15 Eq and Le Chat - Word Search Design Layout References Mailings Review View Help Add i nk Ink to Ink to Drawing Ink Pen Editor Shape Math C anvas Replay Convert Replay Open the Le Chatlier's Principle Activity found in your textbook, Interactive General Chemistry. (Section 15.6, Figure 15.9), run the simulation and complete the following questions. Pens insert 1. Start with the default settings where K - 1.00. a. Write the expression based on...
this example shows the uses of co-coordinate axes, my question is why is it that we...
this example shows the uses of co-coordinate axes,
my question is why is it that we can substitute T for w2 for
the second equation , won t it be wrong since we are using two
different sets of axes
does it have something to do with expressing newtons second
law in terms of magnittude?
can someone explain more about the uses of co-coordinate axes
and when is it not apprioriate not to use it?
5.2 Using Newton's Second Law:...
please answer all parts, thanks!
1. More substituted alkenes are more stable than less substituted alkenes. Show the orbital overlap that helps to explain this observation. 2. Why is the heat of hydrogenation for an alkene exothermic? Analyze the bonds that are changing. AH = -30 kcal/mol Explain: + H2 3. Treating alkene "A" below with HBr can lead to a number of products. "A" SM + H-Br A bunch of products. For real, hella products. 3.A. Label the stereocenters...
pleas help 5,6,7,8,9,10
III IV 5. The product of free-radical halogenation reactions is an alkyl halide. The major amount of this halide forms during the second step of propagation. However, you should be aware that one possible termination step also forms alkyl halides. Why does the majority of the alkyl halide product come from the propagation step and not the termination step? A. At any given time during the reaction, the concentration of both the alkyl radical and the halide...
EXPLAIN IN DETAIL , PLEASE(
LIKE WHERE DO U GET THAT FROM? OR WHY DO WE HAVE TO DO THAT?)
15. Given the enthalpy changes for the following reactions... Equation 1 6MnO(s) + O2(g) → 2 MnO4(s) Equation 2 2Mn2O3(s) + O2(g) → 4MnO2(s) AH° = -464kJ AH° = -142 kJ AH° = -136 kJ Equations 3 Mno(s) + 1/2O2(g) → MnO2(s) It is possible to determine the enthalpy change for the reaction below: "Final Equation" 4Mn304(s) + O2(g) →...
the answers i circled are incorrect except for 19. can you
please tell me why this is correct. can you give me the correct
answers and explain why?
actions usually proceed with amounts of inversion and retention at the center undergoing sustitution more inversion than retention at the center undergoing substitution y more retention then in version at the center undergoing substitution lete inversion at the center undergoing sostituti plete retention at the center undergoing substitution Which of the following...
can you please explain why did he chose the circled product as
a major ?
I only need explaination for part a please
explaination for part A for both questions please
For the following a) Circle the major organic product (1 pt) reaction: b) Provide a mechanism for the initiation and two propagation steps (major only) (5 pts) c) Calculate AH001. AH , and AH (4 pts) d) Which is the rate determining propagation step (1 pt)? Explain (3 pts)...
help please. be as specific as possibly please
-sincerley student in need
all
of the information needed is in the image
Model 7: Which H Will Be Replaced by X? In a radical halogenation reaction a halogen (F, CI, Br or I) replaces an H. In most cases there is more than one type of H to choose from. For example the hydrocarbon below has two different types of H's: CH3 сн CHs hy CH or CH Н-С н,с CH3...
Font Open the Le Chatler's Principle Activity found in your textbook, Interactive General Chemistry. (Section 15.6, Figure 15.9), run the simulation and complete the following questions. 1. Start with the default settings where K = 1.00. a. Write the expression based on the chemical equation in the upper right corner. b. Under the initial conditions of (A) = 2.00 M, and (B) = 4.00 M, is the reaction at equilibrium? How can you tell? c. Compare how Q is affected...
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...
= 1-Lab from Chapter 15 Eq and Le Chat - Word Search Design Layout References Mailings Review View Help Add i nk Ink to Ink to Drawing Ink Pen Editor Shape Math C anvas Replay Convert Replay Open the Le Chatlier's Principle Activity found in your textbook, Interactive General Chemistry. (Section 15.6, Figure 15.9), run the simulation and complete the following questions. Pens insert 1. Start with the default settings where K - 1.00. a. Write the expression based on...
this example shows the uses of co-coordinate axes,
my question is why is it that we can substitute T for w2 for
the second equation , won t it be wrong since we are using two
different sets of axes
does it have something to do with expressing newtons second
law in terms of magnittude?
can someone explain more about the uses of co-coordinate axes
and when is it not apprioriate not to use it?
5.2 Using Newton's Second Law:...
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