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
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- 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 EtOH2) Draw the MAJOR organic products for the following reactions, include stereochem where relevant and there may be more than one product if the reaction would not produce any product, then simply write no reaction in the box provided வி OH Har, High Temp HB, Low Temp Na, CH₂OH 1. R₂BH 2. H₂O₂, NaOH 3Provide the product and mechanism for the reaction: ОН Cro, H,SO, H,0
- eq eq eq [Review Topics] Draw a structural formula for the major organic product of the reaction shown below. Culi CH₂(CH₂)6CH₂Br + на . Consider E/Z stereochemistry of alkenes. • Do not show stereochemistry in other cases. • You do not have to explicitly draw H atoms. • Do not include organocopper or inorganic ion by-products in your answer. 6QQA 85 [References]7A Write the possible products of the following reactions, the mechanism by which they were formed. mentioning Br CH3OH CH3ONa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 4.- Provide the products of the following reactions. As well as the mechanism from which they form H-I H-CI
- Predict the major products of the following reaction. Be sure to show the stereochemistry of the products clearly. Show Transcribed Text Predict the products of this organic reduction: 0 008+ + I xs Cl₂ +1 Pd X X G Click and drag to start drawing a structure. Click and drag to start drawing a structure.a. Enamines formed from the cyclic secondary amine pyrrolidine are important intermediates in the synthesis of 1,5-diketones. On the structures provided below, formation of an enamine from cyclopentanone and piperidine. draw the curved arrows for the reaction mechanism for the acetic acid-catalyzed H H H H eo N H H H3C- isod 1916w Proton Transfer (PT) 000 'H HO :01H SHO 6: HO H H 8²8-- H H 12.H food to shujounte sitt allarWm H OH M HO Nb) 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.
- Suggest a mechanism for the following reactions. Each will require multiple types of concerted pericyclic reactions (cycloaddition, electrocyclic, and sigmatropic. Classify each reaction type. Me3Si Me3Si Me Si Me Sil g HPredict the products and mechanisms of the following reactions. When more than oneproduct or mechanism is possible, explain which are most likely. 2-chloro-2-methylbutane + NaOCH2CH3 in ethanolCH3 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: