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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Propose a mechanism for the reaction of 3-methyl-1-butene with HBr in peroxide. Name and draw the product and determine the stereochemistry. Use arrows to show movement of electrons and use words to describe the elementary steps.
Predict the product(s) and provide the name(s) of the products for the following reactions: H X $R= Br Br I KOH ethanol heat KOH EtOH Heat CH3CH₂O- CH3CH₂OH
デジタル形式で段階的に解決ありがとう!! SOLVE STEP BY STEP IN DIGITAL FORMAT Write 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 present stereochemistry, it must be entered appropriately. EXPLAIN THE REACTION MECHANISM STEP BY STEP HCI + HS. SH + H₂ Ni Raney
人工知能を使用せず、すべてを段階的にデジタル形式で解決してください。ありがとう SOLVE STEP BY STEP IN DIGITAL FORMAT DON'T USE CHATGPT 3.- Provide the products of each reaction and say what type of product it corresponds to (SN1 or SN2). As well as the reaction mechanism from which they are formed. ゾ Br Na CN CH3CH2OH Na OCH₂CH3 EtOH
6A1: Distinguish between synthetic and retrosynthetic transformations to solve problems and predict starting materials and products. Draw any retrosynthetic sequence where a hydroxyl cycloalkane retron can be retrosynthesized into an appropriate cycloalkene, where the cycloalkene can be retrosynthesized into an appropriate cycloalkane halide. While you are allowed to work out this problem synthetically, you MUST report your final response in the retrosynthetic direction using the symbology we learned in lecture/
Predict the major organic products of the following reaction. You do not need to include stereochemistry in your answer. If no significant reaction will occur under the conditions shown, check the box under the drawing area instead. Note: for the purpose of this problem, simple acid-base reactions between the reagents should not be considered a significant reaction. H₂N 7 + 1. LIAI H (OtBu) 2.H₂0 Click and drag to start drawing a structure.
Suppose you are told that each reaction is a substitution reaction but are not told the mechanism. Describe how you could conclude from the structure of the haloalkane, the nucleophile, and the solvent that each reaction is an SN2 reaction.
(a) In an acid-catalyzed hydration, one of the following 10 carbon alkynes is expected to produce a single hydration product? Select the correct alkyne and draw the structure of the hydration product that is formed from this alkyne. (I) 2-decyne; (II) 3-decyne; (III) 4-decyne; (IV) 5-decyne; (V) none of these will give a single hydration product. (b) The reaction shown below gives Compound X as the major product. The mass spectrum of X is shown. Br2, H20 Compound X 100 - MS-IW-5644 80 60 40 - 20 - 20 40 60 80 100 120 140 160 180 200 220 m/z Considering the reactions of alkynes and the MS data, de duce which of following structures corresponds to X: Br Br HO, IV V I II II Support your answer with a reaction mechanism for fomation of X and identification of relevant peaks in the mass spectrum. 12 Relative Intensity
Provide a short answer for why the secondary alkyl halide is the major product versus the tertiary alkyl halide from free radical halogention H₂C NBS H₂C, Br H₂C むーびず H peroxides Br + enantiomer + enantiomer Major Minor
Not hand written please. Give explanation of the correct and the explanation of the incorrect options.

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