Is true about halohydrins, example bromohydrin the intermediate in a. the reaction mechanism is a cyclic halonium (bromonium) ion all b. alternatives are correct c.the product contains a halogen and an OH on adjacent carbons d. the nucleophile (H2O) attacks the most substituted carbon

Q: Draw the mechanism of the  reaction that would occur if water enters your reaction flask while you…

A: Grignard reagent: Grignard reagent is a compound with molecular formula R-Mg-X where, R = alkyl…

Q: What are the products for each of these? What's the whole mechanism for B?

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Q: Use the appropriate reagent used in the reaction. (d),(e) please!!

A: Here we have to mention the appropriate reagent for reaction d and reaction e-

Q: Match each step with the description that best fits it. a)proton transfer b)nucleophilic attack…

A: Each step of reaction with following description are

Q: NaOEt ELOH elimination product 8. Br

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Q: Draw the structure of synthetic intermediate B. F но SOCI2 A B Pyridine

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Q: HOCH2CH2OH catalytic H* Many of the reactions in Chapters 15 and 16, such as acetal formation (shown…

A: The question is based on the concepts of Organic mechanisms. ketones react with ethylene glycol to…

Q: In polar process of the reactions Bond formation is unsymmetrical Bond breaking is homolytic O…

A: Polar reactions occur when two bonded atoms come apart, one taking more of the shared electrons than…

Q: ion was found to E he reaction rate to fo

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Q: The conversion of acid anhydrides to ester via alkoxides is a favorable reaction

A: A question based on introduction to organic chemistry that is to be accomplished.

Q: Label the reactive features of each molecule and then circle the nucleophile used in the reaction…

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Q: Provide the step-wise mechanism for the ffg.. Draw the intermediate/s involved in each rxn. This…

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Q: draw the reaction coordinates comparing using a rxn graph

A: It is given that two reactions are undergoing E1 reactions, and the reaction coordinate diagrams…

Q: Consider the following reaction. cat. ACOH el H2N-NH2 Toluene (reflux, remove H2O) a. Draw a…

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Q: D. Is the nucleophile strong or weak? E. Is the solvent polar protic or polar aprotic? F. What type…

A: Note: polar protic solvent and weak nucleophile and secondary alkyl halide all favors a sn1…

Q: system, ncentration of the H3PO4 will decrease upon addition of KOH. ncentration of the H₂PO4 will…

A: Acidic Buffer solution is the mixture of weak Acid and its conjugate base.  When KOH is added to…

Q: Draw Step 2 of the mechanism. I Edit Drawing

A: The given reaction is a type of Nucleophilic addition followed by substitution.

Q: Draw structures for the carbonyl electrophle and enolate nudeophlle that rea • You do not have to…

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Q: Write the mechanism for the nucleophilic acyl substitution reaction in Figure 40. Generate a SMILES…

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Q: Look at the image below to answer question A-C A. What is the name of this aldehyder. B. Draw a…

A: A. The IUPAC name of the aldehyde is 2-methylbutanal as shown below,

Q: он Br

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Q: 8. Draw the mechanism for this reaction using curved arrows AND box in the major final product(s)…

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Q: Why energy required to reach transition state is lower in active site? And not Lowe in any other…

A: In a particular reaction, the minimum amount of kinetic energy required by the reactant molecule to…

Q: Draw curved arrows to show the movement of electrons in this step of the reaction mechanism.

A: Sequence :-  Protonation of alkene Carbocation rearrangement Attack of methanol as nucleophile…

Q: Add curved arrow(s) to draw step 2 of the mechanism. Modify the given drawing of the product as…

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Q: what one compound would I use as a starting point for the attached reaction?

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Q: Ph Ph МСРВА Но HO.

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Q: Y-Z a. Circle the substitution product. b. Based on the structures of the two products, why do you…

A: Let us discuss the energy level diagrams of substitution and addition reactions.

Q: Explain why alkylation of an α-carbon works best if the alkyl halide used in the reaction is a…

A: The alkylation reaction of an α-carbon depends on the R-X (alkyl halide) used in the reaction. The…

Q: This reaction takes place via a pinacol rearrangement. Draw curved arrows to show the movement of…

A: Sulphuric acid(H2SO4) is used as dehydrating agent which rearranged ketones and also side products…

Q: What major product (from Figure #1) results from the following dehydration reaction (from Reaction…

A: Alcohol gives dehydration reactions when they react with a strong acid like H2SO4 or H3PO4 to form…

Q: Draw the products of attached reaction using the two-part strategy

A: Interpretation: The products of attached reaction using the two part strategy to be drawn.

Q: Draw the neutral organic starting material. Br, CH,CI, Br

A: The neutral organic starting material has to be drawn.

Q: From each pair, select the stronger nucleophile. Q.)Cl- or I- in DMSO

A: The species, that make a covalent bond by donates a pair of electrons is known as nucleophile.…

Q: Add curved arrow(s) to draw step 1 of the mechanism. Modify the given drawing of the product as…

A: 'O' is an electron rich species having lone pair of e- whereas H- is also an e- rich species. Both…

Q: Consider the following Diels-Alder reaction: a) Draw a detailed mechanism for the reaction and show…

A: Since you have asked a multiple sub part question so we have answer first 3 if you want any…

Q: :0: CH H2O Draw H3C Intermediat e nucleophilic addition H2O deproton ation H3O* Draw H- H…

A: The given mechanism is known as acetal hydrolysis or deprotection of carbonyl compound in acidic…

Q: Which is/are NOT TRUE about bimolecular nucleophilic substitution reactions?  Select one or more:…

A: Given,  The False ot NOT TRUE statement about bimolecular nucleophilic substitution reactions is:

Q: An acid catalyst in nucleophilic addition of aldehydes and ketones is used for: Select one: O a.…

A: 1.)  We would use a reaction to predict the use of acid catalyst in the reaction.  2.) Difference in…

Q: In step 7, a hydroperoxide ion reacts with the glycosulose molecule to form a peroxy intermediate.…

A: The functional groups are key components associated with a molecule and are highly responsible for…

Q: Draw structures for the carbonyl electrophile and enolate nucleophile that react to give the aldol…

A: The enolate nucleophile ion in its carbanion form and Carbonyl electrophile.This is intramolecular…

Q: NH2 NH2 TCI AICI3 aniline

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Q: Na HO, Br

A: When an alcohol is treated with NaOH, the following acid-base equilibrium occurs.   The…

Q: What is the stepwise mechanism

A: The reactions involving organic compounds are called organic reactions.  Organic reactions are of…

Q: Draw the products of attached reaction, and state whether the reaction is faster or slower than a…

A: The carbonyl group withdraws electron density from the ring deactivating it towards electrophilic…

Q: Synthetic

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Q: how to know whihc halide is more nucleophilic in a competition reaction

A: In compitition reaction, reactivity is depend upon the nucleophilic power of particular halide.…

Q: A student wanted to dry some diacetone alcohol and allowed it to stand over anhydrouspotassium…

A: In the given reaction the compound was diacetone alcohol which when kept with anhydrous potassium…

Q: Explain Tautomerization with example?

A: Tautomerization

Q: for this reaction scheme suggest a reagent that could be used to accomplish the first step and draw…

A: Alcohols on reaction with sodium metal forms sodium alkoxide . R-OH + Na ------> R-O-Na+ Sodium…

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.