The replacement of bromide ion to the iodide ion as a leaving group in the substitution reaction below results in what?

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

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Q: Select one deactivator & ortho para director to be on a benzene ring to start.  You will then add a…

A: Ortho- para structure on benzene ring is given as follows -

Q: v.. Using curved arrow notation, propose a detailed mechanism that is plausible for the following…

A: This is an example of formation of bromonium ion followed by intramolecular SN2 reaction.

Q: Select one activator & ortho para director to be on a benzene ring to start.  You will then add a…

A: Here, I take -OMe (methoxy) group as an activator.  In case of anisole, the l.p. present on -OMe…

Q: Add curved arrows to draw the first part of the mechanism: tautomerization of a ketone to an enol.…

A: Keto-enol is a type of structural isomerism which involves a keto form (containing C=O) with alpha…

Q: Draw the major product of the following reaction and enter its InChI code in the space provided. OCH…

A: In this question we have to tell the major organic product of the reaction.

Q: Draw the major organic product of the reaction shown below.

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Q: True or false: the carbocation shown will undergo rearrangement. (Show your work and provide a brief…

A: The stability of the carbocation depends on the delocalization of the positive charge and the…

Q: d. Consider the following secondary halides. Changing the leaving group from fluoride to bromide…

A: Halides are good leaving groups. The tendency of the leaving group increases as the size of the…

Q: (CH3),CCI ?

A:

Q: draw the major organic product generated in the reaction below. Pay attention to Regio and…

A: A process that favors bond formation at a particular atom called regioselectivity. solution i)…

Q: For each horizontal row of substituted benzenes, indicatea. the one that is the most reactive in an…

A: Various types of mechanism are studied in organic chemistry. Different organic compounds undergo…

Q: Add curved arrows to draw the second part of the mechanism: tautomerization of an enol to a ketone.…

A: Given the first step of this reaction is the electrophilic addition of deuterium (D).  Second step…

Q: Substitution with a(n) to an aromatic ring would result in reaction? Deactivator group, fast…

A: Activator - electron donating group  and para and ortho directing  Example - OH, OCH3 Deactivator -…

Q: Q1 Complete the following reactions with mechanism ( OCH3 i) + CH3-CH3-CH3-C1 ACl, NO2 dilute HNΟ,…

A: Given: Some of the Reactions are given  To find: To complete the given Reactions with mechanism…

Q: What is the mechanism that leads to the circled, minor product? Is a hydrogen from one of the…

A: The alkyl halides are known for the direct bonding of the halogen to the carbon of the hydrocarbon.…

Q: Which compound will be a major product of the reaction sequence shown below?

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Q: Add two curved arrows to the reactant side to illustrate the movement of electrons in the E2…

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Q: Show a curved arrow mechanism for the formation of the major product below. major minor The…

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Q: Draw the major product of the substitution reaction shown below. Ignore any inorganic byproducts.

A: We have given the organic reaction and we have to find the major product of the reaction.

Q: For the reaction below provide all possible product(s) and circle the major product.

A: This reaction is Aldol Condensation reaction in the presence of acid water. You can see details…

Q: During electrophilic aromatic substitution, a resonance-stabilized cation intermediate is formed.…

A:

Q: エース z-z L H H + CH Anything you need け。

A: Detail mechanistic pathway is given below

Q: The nucleophile approaches from the opposite side of the carbon with the leaving group in which…

A: It is SN2 reaction. In SN2 reaction i.e nucleophilic substitution biomolecular,   one bond is broken…

Q: Which carbon/s of the following compound will give the most electrophilic substitution product?

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Q: Drag the appropriate items to their respective bins. CH3 CH= CH2 CH3 CH3CH(CH3)CH,NH2 CH3CH2COO…

A: Attacking reagents can be classified into two types  Electrophiles (E+)  Nucleophiles (Nu-)…

Q: H2O, H2SO4 H9SO4 A. В. С. E. None of these choices is correct. D.

A: In presence of HgSO4 and H2SO4 , H2O ,oxymercuration-demercuration reaction is carried out and…

Q: What is the starting material in the reaction below?

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Q: Please draw the possible resonance structures for the following carbocations.  Please demonstrate…

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Q: During electrophilic aromatic substitution, a resonance-stabilized cation intermediate is formed.…

A: An electrophile attacks at more nucleophilic site. In case of electron donating group, ortho and…

Q: What is a multi-step synthesis for the following:

A: The final product can be prepared in the following steps:Step 1 : Preparation of alkene from alkyl…

Q: The correct sequence of reactions to carry out the following transformation is:

A: B is the correct option. The Wittig reaction is a chemical reaction of an aldehyde or ketone with a…

Q: Ás written, the following synthesis scheme is flawed. Draw the actual product(s) that would be…

A: In the first step, toluene is first treated with Br2, FrBr3. It is a electrophilic bromination of…

Q: Complete the following: ACONO, Асон, -10°С N. H

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Q: The E2 Mechanism Draw the major and minor elimination products for the reaction of…

A:

Q: The following transformation is an example of a Darzens reaction. Draw its complete, detailed…

A: The Darzens reaction is an organic reaction that takes place between an aldehyde or ketone and an…

Q: CH3 H;C-C-i: CH, CH3 H,C CH,

A: SN1  stands for nucleophillic substitution reaction where rate of the reaction depends on only the…

Q: Which is the correct order of reactivity for the following alkyl bromides in an El reaction?

A: Given : structure of alkyl halide.  Reactivity of alkyl halide is directly proportional to the…

Q: NH2 same molecular formula will be formed. Briefly (i) explain why this compound cannot be isolated…

A: Solution:The class of given compound is enamine in more correct primary enamine. We know primary…

Q: NH2 но. CF3 CF3 IZ

A: The fate of the given reaction is decided by the chemical nature of the leaving group and its…

Q: draw out a detailed mechanism showing the transformation from stilbene to stilbene dibromide C14H12…

A: The reaction taking place is given as, => C14H12 + 2 HBr + H2O2 -------> C14H12Br2 + 2 H2O

Q: Consider the following reaction. In the absence of peroxides, the major product of the reaction is…

A: Since we know that alkene react with HBr in absence of peroxide to form bromo-alkane by ionic…

Q: Reaction C Modify the structure to give the product of reaction C. Draw the counterion. Select Draw…

A: the given molecule is a tertiary amine. We know that tertiary amine has a nitrogen having a lone…

Q: CH,0-P-8 OCH, CH;0O, NaOCH3 H. OCH3 + CH,0 OCH3 CH;OH CH;0 CH;0

A: This is an example of Wittig-Horner reaction

Q: Which of the following synthetic routes is the one that will most successfully generate a.

A: Alpha hydrogens are acidic in nature when base is used it is abstracted and gives conjugate base,…

Q: This reaction is an example of conjugate addition of a nucleophile to an a,ß-unsaturated carbonyl.…

A: The alpha hydrogen to the carbonyl group is acidic in nature and this hydrogen is removed in…

Q: Which of the following alkene addition reactions occur/s specifically in syn fashion?…

A: If we say a reactions occur/s specifically in syn fashion, the adding atoms should be on same side.…

Q: (e) Identify the Michael donor and Michael acceptor that could be used to synthesize this molecule…

A: The reaction in which nucleophilic addition of carbanion to an α,β-unsaturated carbonyl compound is…

Q: Which rearrangement product will form preferentially during the [1,2]-rearrangement of an R-group?…

A: The rearrangement product is stable if the intermediate carbocation formed is stable. We have to see…

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.