Predict the products of this organic reaction:CH3-C-O-CH2-CH2-C-CH3+ H₂O?ASpecifically, in the drawing area below draw the condensed structure of the product, or products, of this reaction. (If there's more than one product, draw themin any arrangement you like, so long as they aren't touching.)If there aren't any products because this reaction won't happen, check the No reaction box under the drawing area.No reactionClick anywhere to draw the firstatom of your structure.:☐d

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Answered: Predict the products of this organic…

Chemistry: The Molecular Science

5th Edition

ISBN:9781285199047

Author:John W. Moore, Conrad L. Stanitski

Publisher:John W. Moore, Conrad L. Stanitski

Chapter6: Covalent Bonding

Section: Chapter Questions

Problem 24QRT

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Alcohols are very useful starting materials for the production of many different compounds. The following conversions, starting with 1-butanol, can be carried out in two or more steps. Show the steps (reactants/catalysts) you would follow to carry out the conversions, drawing the formula for the organic product in each step. For each step, a major product must be produced. (See Exercise 62.) (Hint: In the presence of H+, an alcohol is converted into an alkene and water. This is the exact reverse of the reaction of adding water to an alkene to form an alcohol.) a. 1-butanol butane b. 1-butanol 2-butanone
4) Draw (skeletal) and name the product(s) of the following reactions. If there is a major product, label it as such. If the reaction cannot happen, indicate this. Hydration of cis-2-butene H₂SO,/H₂O
33. Organic compounds undergo a variety of predictable reactions. Complete the following table to demonstrate your understanding of the structures and IUPAC names of organic compounds and the products produced by some of their most common reactions. Reactant(s) (Structures and Names) Propene + Cl2g) Reaction Type Product(s) (Structures and Names) (SATP) Addition (Halogenation) KMNO, in H,SO, нн H-C-C-OH Oxidation FeBr, Br + HBr Substitution
Predict the organic products that form in the reaction below: HO- + H* X H+ Note: You may assume you have an excess of either reactant if the reaction requires more than one of those molecules to form the products. In the drawing area below, draw the skeletal ("line") structures of the missing organic products X and Y. You may draw the structures in any arrangement that you like, so long as they aren't touching. Click and drag to start drawing a structure.
For the following, you must draw an appropriate structure that has the chemical formula C5H7O2Cl with the indicated functional group(s) and/or property. In each case, identify any other functional groups in the molecule you draw, that were not indicated in the question. You may use Lewis or bond- line structures to draw your molecules. You may not use the same structure to answer more than 1 question. a) An acyclic molecule that cannot form hydrogen bonds with itself b) A tertiary chloride c) A cyclic ether
Draw the condensed structure for the major product and indicate if no reaction
Consider the following reactions: a. When C6H14 is reacted with Br2(g) in the presence of ultraviolet light, four different monobromination products form. What is the structure of C6H14 in this reaction? b. When CSH10 is reacted with H2O, a tertiary alcohol is produced as the major product. What is the structure of C5H10 in this reaction? When C6H10 is reacted with HCI, 1-chloro-1-methylcyclopentane is produced as the major product. What are the two possible structures for C6H10 in this С. reaction? d. When a hydrocarbon is reacted with water and the major product of this reaction is then oxidized, cyclohexanone is produced. What is the structure of the hydrocarbon in this reaction? When C4H100 is oxidized, a carboxylic acid is produced. What are the possible е. structures for C4H100 in this reaction?
Write the structure of the compound that will be produced in the following reaction? CH3 –C ≡ C–CH2– CH2 – CH3 + 2HBr→ a) Other than the combustion of alkanes, why are alkanes not reactive, or when they do react, they do so very slowly? B) What chemical reaction can alkenes and alkynes undergo that alkanes cannot? Explain
Question: In an organic chemistry laboratory, a student is performing a reaction to synthesize a compound. The reaction involves the conversion of an alcohol into an alkene using a dehydration process. The student chooses to use concentrated sulfuric acid (H2SO4) as the catalyst for this reaction. However, during the reaction, the student notices that another product is formed along with the desired alkene. (a) What is the likely identity of the unexpected product formed during the reaction? Explain your answer. (b) Provide a plausible explanation for the formation of the unexpected product and suggest a modification to the reaction conditions that would favor the desired alkene as the major product.
Identify the organic functional group(s) of the reactant, the reaction type, and predict the functional group(s) of the product(s) then draw the major product(s) and upload as one file in the last question.The reactant is:The reaction type is:The product should be:
In this organic nomenclature, what does the (4E), "en" and "yl" mean?
An alkene forms 2-methylpropane when catalytically reduced and 1,2-dichloro-2-methylpropane when treated with Cl₂. Draw the structural formula of the alkene. • You do not have to consider stereochemistry. • You do not have to explicitly draw H atoms. • In cases where there is more than one answer, just draw one. / √ [F ? ChemDoodle

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