Draw the structures of all the products that can be formed by the reaction of p-bromotoluene with sodium amide in ammonia at -33 °C. Br NINH, NH, '2' -33°C 3
Q: Answer all questions. Show major products only.
A: Major products for the reactions given:9. 10. 11. 12. 13. 14. 15. 16.
Q: Consider the reaction CO(g) + Cl2(g) CoCl2(g) Using the standard thermodynamic data in the tables…
A: standard delta G = delta G of product - delta G of reactant We need to look up the standard Gibbs…
Q: Part B What is standard pressure? Express your answer in atmospheres as an integer. ΜΕ ΑΣΦ -> P =…
A: Detailed explanation:Now let's explore the idea of standard pressure in more detail: Definition:…
Q: Consider the branched alkane below and complete the following tasks based on its structure. Part: 0…
A:
Q: Draw the product of the following epoxide reaction, including the stereochemistry at any stereogenic…
A:
Q: Gold is frequently purified by electroplating. Typically the gold is dissolved in a cyanide solution…
A:
Q: In an order 1 kinetic reaction, I have the following data table: t/ °C 300 0,00004 200 0,004 How…
A: The equation of half-life for first order reaction is:The rate constant (k) is highly dependent on…
Q: Drawing Lewis Structures For each molecule, calculate the total number of valence electrons. Then,…
A: Step 1:Formal Charge :The formal charge, abbreviated as "FC" is the charge assigned to atoms in a…
Q: Please give a detailed stepwise mechanism for the following reactions. All arrows, charges, and…
A: Approach to solving the question: Detailed explanation: Examples: Key references:
Q: Imagine the main chain of a protein bends back on itself, so that two amino acid residues R₁ and R₂…
A: Can the amino acid residue R₁ form a hydrogen bond with residue R₂ at physiological pH, if R₂ were…
Q: name of this compound????
A: In case of any doubt please feel free to ask.
Q: Part A What is the pH of a solution prepared by dissolving 2.0 g of HCl in water to make 475 mL of…
A:
Q: Which of the carbon atoms shown displays the signal that is the most downfield in the 13C NMR…
A: I : The shift will be around 110- 140 ppmII : The shift will be around 190-220 ppmIII : The shift…
Q: Given the following reaction: 2ICl3 + 3H2O → ICl + HIO3 + 5HCl. If you begin with 15.0 g…
A: Reaction involved is:- 2ICl3 + 3H2O -> ICl + HIO3 + 5HClGiven mass of ICl3 = 15.0 gMolar mass of…
Q: Draw reaction mechanisms to explain the following reactions.
A: Approach to solving the question: Detailed explanation: Examples: Key references:
Q: Please show reaekson and don't use hend raiting
A: Approach to solving the question: Detailed explanation: Examples: Key references:
Q: Chemistry
A: Approach to solving the question: Detailed explanation: Examples: Key references:
Q: None
A: This is an excerpt from an academic journal article about TymeBank, a digital bank in South Africa.…
Q: Calculate (to the nearest 0.1%) the proportion of a dose of ebastine (pKa of conjugate acid = 10.3)…
A: The Henderson-Hasselbalch equation is expressed as: pH = pKa + log([A-]/[HA]), where [A-] is the…
Q: The rate constant of a practically irreversible second-order reaction 2 A → B has a value of 0.145…
A: In solving this problem, integrated rate law for a second-order reaction is used. The integrated…
Q: Part a and b please
A: Step 1: Step 2: Step 3: Step 4:
Q: The equilibrium constant, Kc, for the following reaction Is 10.5 at 350. K. 2CH2Cl2 (g) = CH4(g) +…
A: Step 1: Step 2: Step 3: Step 4:
Q: Assuming the use of the same stationary and mobile phases, how would the Rf of a compound change ifI…
A: Step 1: Information: TLC is a thin layer chromatography It is the analytical techniques that used…
Q: 1. Propose a synthesis for the transformation below. O Ph O Sol-80 CH₂OH
A: Approach to solving the question: Detailed explanation: Examples: Key references:
Q: QUESTION 8 A to C. Give the complete mechanism for the transformation of compound A to B and…
A: Let's start with the reaction of compound A to B: Compound A to B with ( H2SO4 ) and ( CH3OH ):The…
Q: Propose a synthesis route for the reactions below. All reagents and intermediates must be shown.…
A:
Q: Write down the Lewis dot structures of each of the following molecules. Check the formal charge in…
A: Now let's draw the Lewis dot structure for each molecule givena) CH2Cl2 In this Lewis structure,…
Q: Using the blank graph space below, draw an energy diagram/profile for a reaction that includes the…
A:
Q: Dinitrogen tetraoxide is a colorless gas at room temperature. It can dissociate into nitrogen…
A: The equilibrium:N2O4 ←→ 2NO2The expression for equilibrium constant,K = [NO2]2 = constant…
Q: The effect of adding sodium hydroxide and silver nitrate to the FeSCN2+ complexa) Give a balanced…
A: Step 1:, Step 2: Step 3: Step 4:
Q: Question 7 (2 points) According to the chemist system, what is the correct carbon designation for…
A: Carbon Number Assignment of Fatty AcidsFatty acid carbon atoms are numbered starting at the terminal…
Q: Based on the graph, what would you calculate as the sulfate concentration when the net voltage was…
A: Based on the given information, calculating the sulfate concentration at a net voltage of 0.013 V…
Q: Give the IUPAC name of the product formed in the following reaction of ethyl cyclopentanecarboxylate…
A: The reaction is a base-catalyzed hydrolysis of ester or simply saponification.In this reaction, it…
Q: For each atom in the table below, write down the subshell from which an electron would have to be…
A:
Q: The boiling point of water is 100.0°C at 1 atmosphere. How many grams of potassium hydroxide (56.11…
A: Step 1: for moles of KOHwe need to determine the molality of the potassium hydroxide solution. We…
Q: QUESTION 1-DATA ANALYSIS a. Obtain a table expressing concentrations in mg/L and micromole/L ( b.…
A: The question asks you to analyze the data from a potentiometric titration. The data shows the…
Q: QUESTION 1 Combustion of 7.67 g of liquid benzene (C6H6) causes a temperature rise of 47.6 °C in a…
A: Step 1: Calculate the heat absorbed by the calorimeter. qcal = Ccal ΔTwhereCcal = heat capacity of…
Q: None
A: Step 1: Step 2: Step 3: Step 4:
Q: Step by step solution
A:
Q: 3. What is the most likely product of the following reaction? a. I b. II c. III 1. CI 2. Zn/HCI ,…
A:
Q: Optical isomerism in organic compounds (illustrated written account 700) • Compare different…
A: To explore this concept in depth, we can compare the enantiomers L-alanine and D-alanine, which are…
Q: 18. What is the third intermediate of the following reaction? R shown.) a. b. R. R 6-8-0- -0-0-6 R…
A:
Q: None
A: Answer:Step 1:Based on this information, the ideal bond angles are:1) Carbon atom 1 is sp²…
Q: Problem 78 of 80 Submit Curved arrows are used to illustrate the flow of electrons. Using the…
A:
Q: Ca(NO3)2 , CuSO4 Molecular equation Total ionic equation Net ionic equation
A: Steps to write the equations:Step 1:Word equation: The equation which is wrote using the chemical…
Q: Draw the major product of the aldol condensation reaction between two equivalents of this aldehyde…
A: An aldol condensation is a condensation reaction in organic chemistry in which an enol or an…
Q: None
A: Approach to solving the question:By definition, ketohexoses are a class of carbohydrates that have 6…
Q: Solution for the uploaded question please.
A: Given: Soil element strength properties c= 50 kPa, Φ= 15°Required: 3.1 Find σ1 at failure if σ3 =…
Q: Click the "draw structure" button to launch the drawing utility. Complete the reaction below. NBS…
A:
Q: Which of the following refers to oxidation reaction (O), and which refers to reduction reaction (R)?…
A: Step 1: Step 2: Explanation is given step by step manner so that it is easy for you to understand…
Step by step
Solved in 2 steps with 1 images
- What is the major organic product obtained from the following reaction? -- تمرة AICI 3 ب ب میں مجھ IV I OH3C OH OH H+ CH3 Esters can be synthesized by an acid-catalyzed nucleophilic acyl substitution between an alcohol and a carboxylic acid; this process is called the Fischer esterification reaction. Because the alcohol oxygen is a poor nucleophile, the carbonyl carbon is made a better electrophile by protonation of the carbonyl oxygen. The steps of the synthesis are all reversible. The reaction is generally driven to completion by using an excess of the liquid alcohol as a solvent, or by distilling off the product as it forms. Draw curved arrows to show the movement of electrons in this step of the mechanism. Arrow-pushing Instructions CIX 10-4 H₂O CH3 H₂O CH3Describe two ways to prepare the attached compound from benzene.
- Kindly give me complete answers thanks..Draw the major organic product obtained by reaction of benzoyl chloride with dimethylamine, (CH3)2NH.H₂C ཏཱཏི 1 ནི OH 1. Br2, PBг3 2. H₂O H3C OH Br The a-bromination of carbonyl compounds by Br2 in acetic acid is limited to aldehydes and ketones because acids, esters, and amides don't enolize to a sufficient extent. Carboxylic acids, however, can be a-brominated by first converting the carboxylic acid to an acid bromide by treatment with PBr3. Following enolization of the acid bromide, Br2 reacts in an a-substitution reaction. Hydrolysis of the acid bromide completes the reaction. Draw curved arrows to show the movement of electrons in this step of the mechanism. Arrow-pushing Instructions :0: H3C Br Br + :::OH2 Br H₂O H3C Br за
- H8.Identify A, B, and C, intermediates in the synthesis of the five-membered ring called an α- methylene-γ-butyrolactone. This heterocyclic ring system is present in some antitumor agents.In the scheme below, different products are obtained with the reagents given starting from 2-methyl-3-hydroxypentanal. Write the clear structures of the products formed. (A, B, C, D, E, F, G)
- Draw the structural formula of the enol formed in each alkyne hydration reaction; then draw the structural formula of the carbonyl compound with which each enol is in equilibriumPlease give a detailed stepwise mechanism for the following reactions. All arrows, charges, and intermediates must be shown. 1) CN H*, H₂O, heat Яон OHDraw the main organic products of the reaction. Indicate the stereochemistry, including all hydrogen atoms, at each stereocenter. Omit byproducts such as salts or methanol.
