Draw the structure of the product of the reaction between the compound shown below and H2SO4-CH3CH2OH• You do not have to consider stereochemistry.You do not have to explicitly draw H atoms.the reaction involves proton transfer, draw the products in separate sketchers.If the reaction is a Lewis acid-base reaction, draw the product in one sketcher only.VisitedCasteopyChemDoodle®>

The structure of the product of the reaction between CH3CH2OH and H2SO4 has to be drawn.

Answered: Draw the structure of the product of…

Organic Chemistry: A Guided Inquiry

2nd Edition

ISBN:9780618974122

Author:Andrei Straumanis

Publisher:Andrei Straumanis

Chapter20: Acidity And Pka Of Phenols

Section: Chapter Questions

Problem 11E

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Similar questions

Predict the structure of the product formed in the reaction of the organic base pyridine with the organic acid acetic acid, and use curved arroes to indicate the direction of electron flow.
Give a complete curved arrow pushing mechanism for reactions A and B 1) Show ALL important resonance contributors for all intermediates. 2) Add non-bonding electrons and C−H bonds to the line-angle structures as required. 3) Indicate the Lewis acid/Lewis base (LA, LB) at each step as appropriate, and whether they are also Brønsted acids/bases (LA/BA, LB,BB) 4) GIVE THE NUMBER OF STEPS IN YOUR MECHANISM
Compare these two reactions attached, with different Lewis bases and the same Lewis acid. include, at least, kinetic aspect and thermodynamic aspect along with the detailed structural features. show the final products in Fisher projections.
Using the structure of pyridine in the image react pyridine with acetic (ethanoic) acid in a Bronstead-Lowry reaction. Use curved arrows to show the exchange of the proton, and label the conjugate acid base pairs.
Experimental observations show that thiocyanate (SCN- ), the conjugate base of thiocyanic acid (pKa = 1.1 at 25 °C), is quite soluble in neutral water at pH > 2. In the space provided below, explain this experimental observation. That is, why does SCN– readily dissolve in water when the pH > 2?
A mixture of nitric and sulfuric acids generates the nitronium ion,+NO2 (mechanism provided, which can react with benzene to form nitrobenzene vin electrophilic aromatic substitution. Using the provided mechanism that forms the nitronium ion, give a full curved-arrow pushing mechanism for the reaction shown below, indicate the Lewis and Bronsted acids/bases at each step as appropriate (LA LB, BA, BB) and include all important resonance contributors at any ionic intermediates.
For this reaction I attempted to answer them but I got it wrong, and was wondering why? Wouldn't HO- be the bronsted acid since it's accepting the H from the Br, which makes the CH3Br give away the carbon and hydrogens? which is the bronsted acid?
In each of the following reactions, one of the reagents contains two reactive groups (either acidic or basic). You have to decide which group will be affected under mentioned conditions. To answer this problem correctly I suggest that you use the following strategy: (i) Write the products of the reaction: conjugate acid and conjugate base. Use curved arrows to track the flow of electrons; (ii) Using Table 3.1 of the textbook estimate and write pKa values for all acidic groups you have in the reaction equation including conjugate acid; (iii) If you wrote the correct reaction the estimated pKa values should confirm that the reaction transformation changes stronger acid to weaker acid and stronger base to weaker.
Please rank the following by increasing acidity: H2Se, H2O, CH4, H2S
Give only typing answer with explanation and conclusion What are the schemes for the following reactions?: Schemes: 1.Benzoic acid in NaOH 2.Acetic acid in NaHCO3 3.Propan-2-amine in water
Rank each of the following sets of nitrogen bases in terms of basicity and explain your answer
Which species is the stronger Lewis Acid? Why? (Use resonance structures to explain your answer.) BH3 or trimethoxyborate

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