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Specifically explain the differences between the addition of HBr to 1-methylcyclohexene by the ionic mechanism and...
1. Specifically explain the differences between the addition of HBr to propene by the ionic mechanism...
1. Specifically explain the differences between the addition of HBr to propene by the ionic mechanism and by the free-radical mechanism. Differences should include: (a) Reactants (when writing a mechanism be sure to write out (b) Mechanisms complete structures.) (c) Product (may be abbreviated with a line-angle drawing if you wish) differences
2. Provide the complete mechanism (curved arrows) to show how the product is formed. Include all...
2. Provide the complete mechanism (curved arrows) to show how the product is formed. Include all lone pairs, formal charges, curved arrows, intermediates, and products. You do not need to draw the structures of transition states. If there is a carbocation rearrangement and/or a proton transfer, be sure to include it (them) in your mechanism. (Remember to start by drawing all ionic compounds as ions/drawing out the structure of all reagents, and drawing in all lone pairs.) HCI 3. Which...
Please answer all two questions and please explain! I'm completely lost at the moment and I'm...
Please answer all two
questions and please explain! I'm completely lost at the moment and
I'm not sure how to solve it. Please do it step by step if
possible.
10. (10 points) Account for the relative product distribution for the radical bromination reaction shown below. (a) Write the hydrogen abstraction step reaction (radical formation), including the transition state, that leads to each product. (b) Match each reaction to the correct reaction coordinate diagram. Draw the reactants on the energy...
To earn full credit and receive feedback, please show all work for all problems. 1. Circle...
To earn full credit and receive feedback, please show all work for all problems. 1. Circle the compound that is the stronger acid. Explain and justify your choice using a combination of words and chemical structures. 2. Provide the complete mechanism (curved arrows) to show how the product is formed. Include all lone pairs, formal charges, curved arrows, intermediates, and products. You do not need to draw the structures of transition states. If there is a carbocation rearrangement and/or a...
Show lone pairs on all appropriate atoms and the proper flow of electrons. (1) Mechanism #1:...
Show lone pairs on all appropriate atoms and the proper flow of electrons. (1) Mechanism #1: • Predict the products of the following reaction under different temperature conditions. • Show the mechanism for how the two products are formed at different temperatures (include resonance structures if appropriate). • Label the kinetic product and the thermodynamic product. (5 points) -80 °C + HBr 40 °C (2) Predict the product and show the complete mechanism for the following reaction. • Make sure...
I need to know the mechanism for step 1- it should be detailed showing all curved...
I need to know the mechanism for step 1- it should be
detailed showing all curved arrows and the correct molecular
structures for reactants, intermediates, and products. thank you
for your help!
2. Nitration and the Hofmann Rearrangement Monk, K.A.; Mohan R.S. The Hofmann Rearrangement Using Househo Synthesis of 3-Nitroaniline). Chem. Educ. 1999,76,1717 and McElveen, vardinas, K.; Stamberger, J.A.: Mohan. R.S. The Discovery-Oriented Approach Organic Chemistry 1. Nitration of Unknown Organic Compounds.). Chem. 1999, 76,535-536.) Step 1. Preparation of 3-nitrobenzamide...
need help with the boxed bullet point. writing the chemical reaction scheme for the experiment. Synthesis of an A...
need help with the boxed bullet point. writing the chemical
reaction scheme for the experiment.
Synthesis of an Alkyl Halide: A Nucleophilic Substitution Reaction, Part I Pre-lab Assignment for Synthesis of an Alkyl Halide: A Nucleophilic Substitution Reaction, Part 1 1. From The Organic Chem Lab Survival Manual ( edition) by Zubrick • Review pages 201-204: Standard Reflux. • Review pages 127-140: Extraction • Review pages 164-189: Distillation, Simple Distillation. The Distillation Example, and The Distillation Mistake. 2. Read this...
2-methylocta-4,6-dien-1-amine Assignment 1: Draw your molecule from IUPAC name
2-methylocta-4,6-dien-1-amineAssignment 1: Draw your molecule from IUPAC
name Using the given IUPAC name, draw your molecule Complete the cover page (p.1) of your portfolio with the
following:o Structural formula of the moleculeo IUPAC name Use a thin, clear binder or report cover to protect the
portfolio Submit the following in the binder:o Cover page as described above (page 1)Assignment 2: Formula, Molar Mass and Functional
Groups On a page titled Expanded Structural Formula draw the expanded
structure of themolecule.o Show...
Experiment 8 Double Replacement Reactions Background: Some reactions have the net effect of causing the cation...
Experiment 8 Double Replacement Reactions Background: Some reactions have the net effect of causing the cation of each reactant to trade places, forming a compound with the other anion. These reactions are known as double replacement reactions. In the example below (unbalanced equation), the barium and sodium cations switch places so that barium forms a product with sulfate while sodium forms a product with chloride. Note that the formula of each product is determined by the charges of the ions,...
Homework 3: Input Validation 1 Objectives control structures console-based user input using Scanner class writing complete...
Homework 3: Input Validation 1 Objectives control structures console-based user input using Scanner class writing complete programs using two classes: client and supplier 2 User Interface Specification This is a console-based I/O program. Display should go to System.out (print or println) and the program will get user input using the Scanner class. The flow of execution should be as follows: When the program starts, display a one-line introduction to the user Display a menu with 5 options 1. validate zip...
1. Specifically explain the differences between the addition of HBr to propene by the ionic mechanism and by the free-radical mechanism. Differences should include: (a) Reactants (when writing a mechanism be sure to write out (b) Mechanisms complete structures.) (c) Product (may be abbreviated with a line-angle drawing if you wish) differences
2. Provide the complete mechanism (curved arrows) to show how the product is formed. Include all lone pairs, formal charges, curved arrows, intermediates, and products. You do not need to draw the structures of transition states. If there is a carbocation rearrangement and/or a proton transfer, be sure to include it (them) in your mechanism. (Remember to start by drawing all ionic compounds as ions/drawing out the structure of all reagents, and drawing in all lone pairs.) HCI 3. Which...
Please answer all two
questions and please explain! I'm completely lost at the moment and
I'm not sure how to solve it. Please do it step by step if
possible.
10. (10 points) Account for the relative product distribution for the radical bromination reaction shown below. (a) Write the hydrogen abstraction step reaction (radical formation), including the transition state, that leads to each product. (b) Match each reaction to the correct reaction coordinate diagram. Draw the reactants on the energy...
To earn full credit and receive feedback, please show all work for all problems. 1. Circle the compound that is the stronger acid. Explain and justify your choice using a combination of words and chemical structures. 2. Provide the complete mechanism (curved arrows) to show how the product is formed. Include all lone pairs, formal charges, curved arrows, intermediates, and products. You do not need to draw the structures of transition states. If there is a carbocation rearrangement and/or a...
Show lone pairs on all appropriate atoms and the proper flow of electrons. (1) Mechanism #1: • Predict the products of the following reaction under different temperature conditions. • Show the mechanism for how the two products are formed at different temperatures (include resonance structures if appropriate). • Label the kinetic product and the thermodynamic product. (5 points) -80 °C + HBr 40 °C (2) Predict the product and show the complete mechanism for the following reaction. • Make sure...
I need to know the mechanism for step 1- it should be
detailed showing all curved arrows and the correct molecular
structures for reactants, intermediates, and products. thank you
for your help!
2. Nitration and the Hofmann Rearrangement Monk, K.A.; Mohan R.S. The Hofmann Rearrangement Using Househo Synthesis of 3-Nitroaniline). Chem. Educ. 1999,76,1717 and McElveen, vardinas, K.; Stamberger, J.A.: Mohan. R.S. The Discovery-Oriented Approach Organic Chemistry 1. Nitration of Unknown Organic Compounds.). Chem. 1999, 76,535-536.) Step 1. Preparation of 3-nitrobenzamide...
need help with the boxed bullet point. writing the chemical
reaction scheme for the experiment.
Synthesis of an Alkyl Halide: A Nucleophilic Substitution Reaction, Part I Pre-lab Assignment for Synthesis of an Alkyl Halide: A Nucleophilic Substitution Reaction, Part 1 1. From The Organic Chem Lab Survival Manual ( edition) by Zubrick • Review pages 201-204: Standard Reflux. • Review pages 127-140: Extraction • Review pages 164-189: Distillation, Simple Distillation. The Distillation Example, and The Distillation Mistake. 2. Read this...
2-methylocta-4,6-dien-1-amineAssignment 1: Draw your molecule from IUPAC
name Using the given IUPAC name, draw your molecule Complete the cover page (p.1) of your portfolio with the
following:o Structural formula of the moleculeo IUPAC name Use a thin, clear binder or report cover to protect the
portfolio Submit the following in the binder:o Cover page as described above (page 1)Assignment 2: Formula, Molar Mass and Functional
Groups On a page titled Expanded Structural Formula draw the expanded
structure of themolecule.o Show...
Experiment 8 Double Replacement Reactions Background: Some reactions have the net effect of causing the cation of each reactant to trade places, forming a compound with the other anion. These reactions are known as double replacement reactions. In the example below (unbalanced equation), the barium and sodium cations switch places so that barium forms a product with sulfate while sodium forms a product with chloride. Note that the formula of each product is determined by the charges of the ions,...
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