デジタル形式で段階的に解決ありがとう!!SOLVE STEP BY STEP IN DIGITAL FORMATWrite the products of the following reactions, if there is more than one product,enter them and indicate which is the majority and if the compounds presentstereochemistry, it must be entered appropriately.EXPLAIN THE REACTION MECHANISM STEP BY STEPمله1) NaBH4CH32) H₂O+CH3NaAlH4NH₂

Answered: デジタル形式で段階的に解決ありがとう!! SOLVE STEP BY…

Chemistry

10th Edition

ISBN:9781305957404

Author:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste

Publisher:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste

Chapter1: Chemical Foundations

Section: Chapter Questions

Problem 1RQ: Define and explain the differences between the following terms. a. law and theory b. theory and...

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Predict the product of the following organic reaction: CH₂ CH O || C–CH2–CH=CH—(CH2)3 CH3 (CH₂)3 CH=CH- - CH₂ CH3 + 4 H₂ Ni CH,−O -C–CH2–CH=CH–CH=CH–CH2–CH3 Specifically, in the drawing area below, draw the chemical structure of the product P. If there is no product, because this reaction won't happen, check the No reaction box under the drawing area. Click and drag to start drawing a structure. × Ś +
(b) Write the mechanism for the formation of products in following reaction. Clearly show the intermediates in the reaction. Which product is a kinetically controlled and which one is the thermodynamically controlled product? CH3 CI. CI. A½O3, HCI H Ph-C=C-CH3 Ph CH3 Ph H.
7A Write the possible products of the following reactions, the mechanism by which they were formed. mentioning Br CH3OH CH3ONa
Predict the products and mechanisms of the following reactions. When more than oneproduct or mechanism is possible, explain which are most likely. isobutyl chloride + AgNO3 in ethanol>water
Describe the reaction mechanism for the hydrolysis of 2-bromo-2-methylpropane [CH3C(CH3)2Br] with aqueous hydroxide ions (OH-).
CH3 CH3 Br- Br2 CH2CI2 CH3 CH3 H3C H3C Br Electrophilic addition of bromine, Br2, to alkenes yields a 1,2-dibromoalkane. The reaction proceeds through a cyclic intermediate known as a bromonium ion. The reaction occurs in an anhydrous solvent such as CH2C12. In the second step of the reaction, bromide is the nucleophile and attacks at one of the carbons of the bromonium ion to yield the product. Due to steric clashes, the bromide ion always attacks the carbon from the opposite face of the bromonium ion so that a product with anti stereochemistry is formed. Draw curved arrows to show the movement of electrons in this step of the mechanism. Arrow-pushing Instructions CH3 CH3 Br- .CH3 .CH3 H3C H3C :Br :Br:
Fill in the red box(es) with the missing reactant(s), reagent(s), product(s), solvent, and/or conditions and write a reasonable mechanism for the reaction. Not every box need be used and not every box necessarily corresponds to only a single species. If no reaction occurs OR no reagents exist to perform the reaction state, "NOT POSSIBLE" AND explain why. OH O,N "ON N(CH,CH,), Your Answer:
Pericyclic Reactions: Convert 1a to 1b Indicate what type of reactions and mechanisms occured in each step. Indicate reagents/conditions.
3) Fill in the red box(es) with the missing reactant(s), reagent(s), product(s), solvent, and/or conditions and write a reasonable mechanism for the reaction. Not every box needs to be used and not every box necessarily corresponds to only a single species. If no reaction occurs OR no reagents exist to perform the reaction state, “NOT POSSIBLE” AND explain why. H₂O*
Peroxides are often added to free-radical reactions as initiators because the oxygen–oxygen bond cleaves homolytically rather easily. For example, the bond-dissociation enthalpy of the O¬O bond in hydrogen peroxide (H¬O¬O¬H) is only 213 kJ>mol (51 kcal>mol). Give a mechanism for the hydrogen peroxide-initiated reaction of cyclopentane with chlorine. The BDE for HO¬Cl is 210 kJ>mol (50 kcal>mol).
b) Refer to the following equation to answer Q3b (i), (ii) and (iii). CH3 H,SO, Н—с—он C-CH3 ? + H2O Но- ČH3 (i) Determine the product of the above reaction. (ii) Name the above reaction. (iii) Propose the mechanism for the above reaction.
Each of the following reaction sequences has at least one issue that would either prevent the products from forming as shown or greatly diminish their yield. Identify the issue(s) and briefly explain how the conditions could be modified to allow each reaction to form the products shown. NH₂ Br₂ FeBr 3 t-BuCl AICI 3 NH₂ Br

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