+ 2 MeOH H",

Q: synthesising this molecule with the given reactant

A:

Q: The structure of 5-fluorouracil is shown in the box at the side of the page. Is…

A: 5-Fluorouracil is a heterocyclic aromatic organic compound with a structure similar to that of the…

Q: to carry out the following conversion. Then, perform an additional reaction, continuing onto the…

A: Given reaction is :  Convert the following conversion ?  According to Anti-Markovnikov's rule,…

Q: Protectim of C=0 TSOH benzene HO reglux TS OH =

A: In presence of acid diol can protect carbonyl group.

Q: Classify the attached transformation as substitution, elimination, or addition.

A: In the given transformation, the given reactant does not support addition reaction because all…

Q: Using the template structure of sesamin below, label the sets of equivalent hydrogens as H1, H2, H3,…

A: Chemically equivalent nuclei are those which include nuclei present in similar environments. In…

Q: HO H2SO4

A: In elimination reaction a species leave the substrate and double or triple bond is formed.

Q: For the dehydration shown, use curved arrows to show the formation of the carbocation intermediate…

A: Interpretation- To draw the structure of major product on the elimination reaction which is given in…

Q: h) Ph ÖR Ph Ph Ph Ph (radical initiator) RO, Ph

A: Radical mechanism of styrene

Q: Seachione Prowide the struchured of the expected major organic productisl. Show stereochemistry…

A: Since you have posted multiple sub-parts, but we will be able to solve first three subparts for you,…

Q: Reacting an internal alkyne with H2 in the presence of a Pt catalyst produces

A: Given :-  Internal alkyne + H2/Pt →  To determine :- product of this reaction

Q: 5. Provide a complete, arrow-pushing mechanism which explains the observed re Br CH;CH2OH for

A: Organic reaction mechanisms.

Q: Draw the mechanism for oxymercuration-demercuration  with the following alkene. 2-methyl-1-butene

A:

Q: Use cycloaddition reactions to propose a synthesis of the molecules sho CO,Me LMe Me čO,Me ÓH

A:

Q: From Cyclopentane `CO2H CO2H

A:

Q: Complete the following synthesis route indicating the structures that are missing. .CI H2 Pd/C SnCl4…

A:

Q: (b) What are oxidative addition and reductive elimination steps in a catalytic eycle?

A: 1. Oxidative addition is a process that increases both the oxidation state and coordination number…

Q: NaOH (d) * include stereochemistry

A: An organic compound in which a halogen atom and hydroxide group are attached to adjacent carbon…

Q: Mechanism. Provide the complete mechanism for the reaction below. You must include appropriate…

A: Interpretation- We have to provide the complete reaction mechanism for the given reaction as above…

Q: (d) Carry out the following conversions and provide the mechanism : CH3 HO H3C CH3 -CH3 from H3C H3C…

A: alpha keto carbanions and p-benzoquinoes react to give the product

Q: In the monochlorination ethane, amount 2-chloro bu tone form. Prapose to a small mechanism explain…

A: Halogenation of alkanes proceeds by the free radical substitution reaction. The steps involved are…

Q: 1: NaOH 2: D;SO4 S-Methyl 3-methylbutanethioate

A: The reaction of carbonyl compounds with NaOH results in (SR) nucleophilic substitution reaction.…

Q: what are the limitations of Williamson's synthesis?

A: In addition, the halides which undergo E2 elimination is tertiary alkyl halides or sterically…

Q: А. нно нн В. `CI С. HO CI

A:

Q: H2SO4

A:

Q: ene, C2H2, any four or fewer carb- eptable synthesis of the compou H

A: Required reagent for the Synthesis of give Product. 1- NaNH2, liq. NH3  NaNH2 is a stronger base  2-…

Q: Indicate the possible product of the following reaction:

A: Periodninane is oxidising agent it oxidises primary alcohol into aldehyde and secondary alcohol…

Q: Draw a complete arrow pushing mechanism that explains the following: Br NBS hv Br

A: N-bromosuccinimide (NBS) is used as allylic brominating reagent. 3,3-dimethylcyclohexene on…

Q: Shown here is a carbohydrate: OH HO HOOH Complete this drawing of the straight-chain form of this…

A: In this question, we have to find out the correct answer of given problem by the help of the…

Q: Classify attached transformation as substitution, elimination, or addition.

A:

Q: Complete the mechanism of hydration of alkene below. Please follow curved arrows to predict the…

A: Answer:- The hydration of alkene gives the corresponding alcohol according to Markovnikov rule which…

Q: OH SOCI2 pyr

A:

Q: Draw the products of attached reaction.

A: The sulphonation reaction of anisole can be at ortho and para position. The inductive effect being…

Q: Draw curved arrows to show the movement of electrons in this step of the mechanism. Arrow-pushing…

A:

Q: For this problem, draw all hydrogen atoms explicitly. Part A Draw the product of the hydrogenation…

A: The hydrogenation of ethyne will reduce the ethyne molecule and convert it into ethane molecule by…

Q: Calculate IHD ox degre of unsaturation.

A:

Q: Complete the following transesterification reaction

A: Transesterification is the reaction of the exchange of organic groups between ester and alcohol to…

Q: H3C-C-0-Ĉ-CH3 A FeBr3 + Br2 B (Para Product only) AICI3

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

Q: NaH + CI- NaCl DMF

A: NaH is a strong base. ,so it will produce H- ,Which will try to abstract acidic H of alcohol are as…

Q: Show the Drawing a Dehydration Reaction with a Rearrangement ?

A: The dehydration reaction has to be shown.

Q: Which reactions have a positive ASrxn?

A:

Q: (d) Complete the following reaction: hv (i) Cp2TiMe2 +2 [RCH=CHR] AlMez (ii) [Cp*Ir"Cl}]2 (iii)…

A: NiCl2(PMe3)2 + RMgCl → ?

Q: Add any remaining curved arrow(s) to complete step 4 of the mechanism. Modify the given drawing of…

A: The reaction mechanism step given is,

Q: Draw curved arrows to show the movement of electrons in this step of the mechanism. Arrow-pushing…

A:

Q: Study the curved arrows in the reaction and provide the line structures of all the intermediates and…

A:

Q: hemisn broduet Pdca of kOH (3) BCOH)2 K Br

A:

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.