How the following transformation can be caried out in a most efficient manner. OH Select one o. Tratment with Iodine and concentrated aqueous NaOH sohution, followed by acidification. O a Treatment with KM1O4 in aqueous NaOH solution, followed by acidification. o Treatment with MCPBA. followed by alkaline hydrolysis. • 4 Treatment with Tollen's reagent followed by neutralisation.

Q: Br

A: The important information to note for the given problem is:   It specifies the need of Wittig…

Q: lease show detailed mechanism how this transformation is achieved

A: Oxymercuration-demercuration is the electrophilic addition reaction to alkene. This addition takes…

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: Draw a complete, detailed mechanism for the following 1. R'—ОН, Н reaction. R-C=N 2. H20, НО R OR'

A: The above reaction is an acid catalyzed reaction of nitrile with an alcohol which results in the…

Q: For each set, which of the following compounds will undergo an EAS reaction faster? Explain. a) b)…

A:

Q: From the figure above, what do you expect to observe in these reactions? Which mechanism? Which…

A: It is given that there are three alkyl bromides and two reagents A and B. Which reagent is best for…

Q: •OH H*

A: The objective of this question is show the mechanism of formation of diimidazole ring. The starting…

Q: Provide a synthetic pathway for the following transformation and draw intermediate structures. The…

A: Decarboxylation occur when carbanion is stabilized after leaving CO2....

Q: For each reaction, draw the complete, detailed mechanism and the major product. NaCl HCI ?

A: Reaction of 2-phenyloxirane with nucleophiles is being considered.

Q: Draw the complete mechanism for the reaction below, including stereochemistry.

A: H2SO4 and H2O act as dehydrating agent on double bond.  Mechanism steps  In first step, alkene…

Q: Identify first if it is SN1/SN2 or E,/E, Predict the major substitution product. Identify first…

A: Let us try to understand SN1 vs SN2 and E1 vs E2. Then we can solve the reactions.

Q: please explain along the answer. rate K2CR2O7 H2SO4 / H2O heptanal

A: Reaction of heptanal with K2Cr2O7 in presence of H2SO4 / H2O

Q: Which compound will undergo Sn2 substitution the slowest? CH3CI CH3CH2CI CI CI

A:

Q: PROBLEM How might you carry out the following transformation? More than one 20-12 step is needed.…

A: The objective of the question is to understand the chemical transformation process of converting a…

Q: 5) Only one product is observed in this reaction. Draw the product and briefly explain why. Hint: It…

A: We have to predict the correct product of the given reaction.

Q: When Is the Mechanism E1 or E2?

A:

Q: Draw this reaction's mechanism. It is 1,4-addition mechanism.

A: Step 1: Step 2: Step 3: Step 4:

Q: ZI 1. NaH 2. CI

A:

Q: 6. Determine whether each reaction occurs by an SN2, SNI, EI, and/or E2 reaction. Provide a detailed…

A: The higher the temperature, the more likely elimination occurs. The lower the temperature, the more…

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

A:

Q: HO HO но SH

A: Nucleophilicity is an ability of the particular nucleophile to attack on the electrophilic center.

Q: Radical halogenation generally yields a mixture of stereoisomers. When a Br atom is adjacent to the…

A: In the presence of sunlight, halogenation of the given compound occurs via radical formation. All…

Q: N. Br2/FeBr3 CO2CH3 So,/H2SO4 HO. AICI3 NO2 HNO3/H2SO4 CN

A: Reaction 1 : EAS Bromine is electrophile. Reaction 2 : EAS SO3 is electrophile. Reaction 3 : Fridel…

Q: Show the mechanism and show major products for these two reactions

A: A question based on reaction mechanisms. A reactant and reaction condition are given whose product…

Q: Br AlBr3 CH3

A: An arrow always depicts from a region of high electron density to low electron density ; that is…

Q: b. 0 OH OH (excess) H₂SO4 (cat)

A:

Q: Determine the mechanism of nucleophilic substitut a. Br + -CN acetone b. + -OCH3 C. + CH3OH Br H Br…

A:

Q: From the scheme below, draw the structures of X and Y. These two compounds are the major products of…

A: The reaction of alcohol with strong acid like H2SO4 takes place via E1 elimination reaction. In the…

Q: 10. Predict the major product for each of the following reaction, and draw the complete mechanism.…

A:

Q: Draw arrows to show a typical SN1, SN2, E1 and E2 reaction

A:

Q: In EAS bromination reaction directly on aniline, there will be multiple products including ones in…

A: "Bromination reaction directly on aniline, there will be multiple products including ones in which…

Q: цо что TMS CI OTMS сизмде Изо+ НО 0TMS F- Иго э цо он a

A:

Q: НО NaOH (CH3),N (CH3),NCH,CH,CI Can you show this mechanism please?

A: Nucleophilic substitution biomolecular reaction (SN2): The bimolecular nucleophilic substitution…

Q: Draw all of the steps of the mechanism for this reaction: && H₂SO4 + CH₂OH OH H OCH3 + H₂O

A: We have given the organic reaction and we have to Give detailed mechanism with explanation needed.…

Q: HO, OH

A: The answer is given as follows

Q: The reaction shown here is an example of a deiodination. Without AlCl3 present, no reaction occurs.…

A:

Q: 맛 Hel 디 몇

A:

Q: 2. Show the complete mechanism for the following transformation H*, H20

A: The reaction taking place is given as,

Q: 1. Predict the product/s of this reaction and draw the complete, detailed mechanism. Pay attention…

A:

Q: Show a possible pathway and include all intermediate and reagents.

A: Synthesis of 2-bromo-2-methylbutane from 3-methylbutanol:

Q: If H1 is eliminated from the carbocation shown here in an electrophile elimination step, then three…

A: In E1 mechanism, a carbocation is formed first and then a double bond by the abstraction of proton.…

Q: Which mechanism is going to predominate under these conditions? A SN1 SN2 Br NaOC(CH3) or t-buOH E1…

A: The reaction given is,

Q: Propose a full mechanism using curvy reactions arrows for the following transformation

A: From given structure  Full mechanism including curved arrows is shown below

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.