Please help me, I have the mecahnism good but I am very confused on what the intermediate and product will be

Q: Problem: Would the following transition state lead to a successful reaction? Explain your answer. H…

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Q: Please illustrate mechanism and product NH, HO Br

A: Alcohol is a weak acid and it reacts with a base to form alkoxide ion. The given compound contains…

Q: In step C, which mechanistic step(s) is(are) taking place? Choose all that apply Nucleophilic attack…

A: Here we are required to find mechanism occurring in the different stages of the reaction.

Q: What is responsible for the overalkylation of ammonia? Each alkylation produces a more…

A: In a chemical reaction, reactants undergo a reaction forming the products. Ammonia is a good reagent…

Q: 3. Which of these two reactions would go better? Why? N3 CH3CCH3 CH3 Br CH3CCH3 CH3 CH3CH₂CH₂Br NaN3…

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Q: 1) For the following transformations involving one elementary step each: (i) Draw &+ and 8- on the…

A: Given,

Q: •OH H*

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Q: As some of you have seen while reading/watching outside sources, most textbooks say that SMI and El…

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Q: Me Oz C Me Oz C

A: Wittig reaction is the reaction of an aldehyde or ketone with the ylide generated from a phosphonium…

Q: Question 3 Draw the mechanism and final product for the following reaction. IR (cm-1): 3307, 3295,…

A: There is error in last step only. As N has one H left so when H2O will leave and N shares its lone…

Q: Chlorine and bromine react in the dark with alkenes. The reaction shown below affords a single major…

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Q: 3. Show the mechanism and any intermediates formed in the following reaction. d A

A: retro-Diels-Alder and Diels-alder

Q: CI (CH3)3CONa DMF ?

A: In the given reaction solvent is polar aprotic and base is strong and bulky. So, it will favor E2…

Q: Show the Mechanism for each of these reactions with their MAJOR and MINOR products

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Q: Curved arrows are used to illustrate the flow of electrons. Use the reaction conditions provided and…

A: The objective of the question is to predict the product formed in the following reaction…

Q: (Intermediate) Reactant :ÖH :Br-H Tip: Only add curved arrows in this sketcher Apply Mechanism Hint…

A: In this reaction, the reactants are the hydroxide ion (OH-) and the bromohydrin (Br-H). The…

Q: Draw all products for each of the following reactions or reaction sequences. For chiral molecules…

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Q: Draw all products for each of the following reactions or reaction sequences. For chiral molecules…

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Q: [References] raw the structure of the product obtained when this amine is treated with excess…

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Q: 1) For the following transformations involving one elementary step each: (i) Draw &+ and 8- on the…

A: Elementary step means reaction taking place in a single step.

Q: Identify the product of the following one-step sequence. Note that this is a reaction that you have…

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Q: by the number of the third intermediate, etc., until you have selected the correct intermediates and…

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Q: e) Changing the leaving group from F to I would increase the rate of which mechanisms? Circle ALL…

A: SN1-: SN1 ( nucleophilic substitution unimolecular reaction) occur mostly in two steps.  In step-1…

Q: 7. Draw the complete, detailed mechanism (curved arrows) for the following reaction. No need to draw…

A: Ketone is an electron withdrawing group (EWG), so in electrophilic aromatic substitution reaction it…

Q: Draw the appropriate Newman projection which leads to the major E2 ELIMINATION product. Hint: Review…

A: Step 1:As we know that for E2 elimination, the hydrogen and the leaving group must be anti…

Q: help please answer in text form with proper workings and explanation for each and every part and…

A: Option D : correct answer and it is solved and explain in detail

Q: earning Target 9 citeria for satisfactory score ementary mechanistic steps must be correctly…

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Q: Draw the mechanism for Llle Lll աայււմ 11 i) This mechanism requires 6 steps. ii) Make sure you draw…

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Q: For this structure, draw a mechanism that includes all resonance structures for any intermediates on…

A: Given is organic reaction.The given reaction is isomerisation reaction.Due to the presence of…

Q: Draw the first step in the mechanism for the acid-catalyzed hydrochlorination of the alkene in the…

A: Alkenes are unsaturated organic compounds that have double bond.They are reactive due to the…

Q: The reagent is hydroxide, which is both a strong base and a strong nucleophile. The substrate is…

A: The predicted products can be recognized as follows, since the highly substituted alkene with a…

Q: Draw the starting alkyne that would lead to this major product under these conditions. Drawing HBr…

A: When alkyne reacts with excess HBr it produce geminal  dihalide .Hence, substrate must be Alkyne .

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Q: (Intermediate) Reactant Xe Br: & + Na+ Tip: Only add curved arrows in this sketcher Apply Mechanism…

A: We have given reactant having a good leaving group which is Bromine and a strong base .  Strong base…

Designing a Synthesis

Organic synthesis is a branch of chemical synthesis that involves the planned construction of organic compounds/molecules from smaller units that possess functional groups. Friedrich Wöhler was the first scientist who designed the synthesis of an organic compound, urea from inorganic starting materials silver cyanate with ammonium chloride via a simple, one-step synthesis.