HCI A CH30 CH;O

Q: (a) * ОН ОН _OCH3

A:

Q: Provide the products formed when cyclohexanone and cyclohexanecarbaldehyde reacts with the following…

A: Aldehyde and ketones react with RMgX which is Grignard reagents to form corresponding alcohols.…

Q: Propose a mechanism and predict the major product. Cl2 hv

A: The reaction between alkanes and Cl2 in presence of light i.e hv is known as chlorination reaction.…

Q: i. butanoic anhydride + sodium hydroxide j. butanoyl bromide + potassium ethoxide chs-CHz- CHz- ċ-Br…

A: When an acid or its derivative reacts with alcohol or its derivative, there is a formation of ester…

Q: 17. OH P+ + Hz t > CH3 CHCH, CH2 CHy

A: H2/Pt give reduction of aldehyde and ketone but not give the reduction of carboxylic acid . And this…

Q: 1. Propose a synthetic route for the desired products. a. b. &=&m OH OH HO CH3 OH

A:

Q: 3. The following reaction is used in the industrial synthesis of the antiviral drug, oseltamivir…

A: mechanism for this transformation

Q: HO

A: In the given reaction the cyclohexanol is oxidized into cyclohexanol. The oxidation of the secondary…

Q: Show the product expected when the following unsaturated 8-ketoester is treated with each reagent.…

A: The product of the given reaction can be shown as

Q: 85. a. Propose a mechanism for the following reaction: CH30 + Br Br

A: mechanism is follows as:

Q: 3) Draw a plausible mechanism for the following transformation: 0. 0. H³0Ⓡ NO₂

A: In this question we have to tell the product of the reaction and also its mechanism.

Q: 20. Propose an efficient synthesis for the following transformation: OH ÓH

A:

Q: Propose a mechanism to account for the following reaction CH3 cha nahod CH₂Cl AICH H₂C

A: We have to propose a mechanism for the given transformation. The given reaction is an example of an…

Q: NaOH

A:

Q: Rank the following substituted phenols in order of increasing acidity, and explain your answer

A: Given: We have to arrange these compounds in the order of increasing acidity.

Q: Propose a mechanism for the following: CI HC a. Br HBr b. OH [H*] C.

A: Note: We can solve only first three subparts (as per bartleby guidelines) so, please upload the rest…

Q: Claisen rearrangement of an allyl phenyl ether with substituent groups in both ortho positions leads…

A:

Q: Propose a mechanism for each of the following reactions:

A:

Q: Propose a mechanism (step by step) for the following transformation. Explain each step. HO. H,SO,…

A: Alkenes contain loosely bonded pi-electrons. In the presence of an acid, the alkenes are protonated…

Q: Identify the needed reagents in the following scheme: Br CH2OH HO OH сно b. C. а. d. е. f. -1

A: here cyclohexanone is undergoing certain chemical reaction using different reagents to form trans…

Q: Propose a mechanism for the following reaction. ОН H2SO4 heat

A: Interpretation-  To propose a mechanism for the given following reaction .    Introduction- Here in…

Q: 4. What carbonyl compounds give the following alcohols on reduction with LIAIH4? Show all…

A:

Q: Propose a mechanism for the following reaction:

A: Given reaction is

Q: CO,Me MeOH H;O+ Br

A: Synthetic organic chemistry involves the conversion of the reactants into the appropriate products…

Q: Arrange the following compounds in INCREASING reactivity towards Nucleophilic Acyl Substitution. ABC…

A: Given compounds are organic compounds as they contain carbon and hydrogen atoms.

Q: Propose a mechanism for the following reaction

A: Aldol reaction: It is a reaction in which carbonyl group reacts with enolate of aldehyde and ketone…

Q: `OH ZI

A:

Q: 7. Propose a mechanism for the following transformation. H* `NH2

A: In the mechanism of the above reaction ; 1st step involves the protonation  2nd step : attack on…

Q: Propose a mechanism for the following reaction: H. NaOH H20

A: Michael addition,followed by ring opening and then ring closing will give the product

Q: Propose a stepwise mechanism for the following reaction of a β-keto ester. Suggest a reason why this…

A: The stepwise mechanism for given reaction is shown below, First step is formation of enolate. The…

Q: 5 mol % NAOH

A:

Q: OH H;O +

A:

Q: Propose a synthesis for each ketone, using as one step in the sequence a Claisen condensation and…

A: The given chemical reaction is, The sodium ethoxide would abstract an alpha hydrogen from the…

Q: a. Propose a mechanism for the following reaction.b. Explain why two products are formed.c. Explain…

A: The above reaction takes place via SN1 mechanism because the intermediate formed here is a stable…

Q: Provide a mechanism for the following transformation: CN 1. NaOH CO,H 2. H,O*

A:

Q: 7. Propose a mechanism for the following transformation. EtO,C. CO,Et + NH3 OEt H.

A:

Q: Draw a mechanism for the following transformation: OH ОН Dilute (a) (b) H2SO4 OH [H"] (c)

A: The hydration of an alkene in an acidic medium gives the corresponding alcohol. The first step is…

Q: `N' .N. H20

A: Please find the below attachment.

Q: Propose an efficient synthetic approach using diethyl malonate as one of the reagents for the…

A: This is an basic organic reaction.  The synthesis can be done in 2-3 steps.

Q: CI HCI + H2O

A: In this question we will write a mechanism see below.  1- In the first step carbocation intermediate…

Q: Propose a mechanism for each of the following reactions

A: The organic reactions are carried out with the help of various reagents. This helps in the…

Q: Identify the reagents "a" in the following scheme: OH CH3 CH3 CH3 b. NaOCH3 with acid @ low…

A: In the elimination reaction, the formation of alkene takes place. there will elimination of a proton…

Q: Propose a mechanism for the following transformation CI HCI H2O +

A: Alcohol reacts with an alkyl halide to form an alkyl chloride. The reaction proceeds with an SN1…

Q: Reaction of p-cresol with two equivalents of 2-methylprop-1-ene affords BHT, a preservative with…

A:

Q: Propose a mechanism for the following reaction. acid HC CH + CH3NH, + 2 H2O CH3

A:

Q: .N. 25°C

A: Mechanism of Reaction 1 -

Q: Propose a mechanism for the following reaction

A: Carbonyl carbon is electron deficient in nature due to electronegative oxygen atom bonded to it.…

Q: Propose a mechanism for each of the following reactions:

A: The mechanism for the reaction (a) is shown below.

Q: Propose a synthesis for the following transformation. OEt H' HO,

A:

Aromatic Compounds

Aromatic organic compound or aromatic system is an important class of hydrocarbons under the branch of organic chemistry. Aromatic compounds are also called arenas. The definition of aromatic organic compounds can be stated as a class of organic compounds with a planar cyclic ring of atoms bonded through alternated single and double bonds. Due to these alternating bonds, a peculiar feature termed as ‘resonance’, that is, delocalization of pi electrons or the electrons is shared within the atoms of the ring which are present in the aromatic compounds. The word ‘aromatic’ includes a Greek word ‘aroma’ which means smell, indicating that they were named as such due to the sweet odor they produce. Many well-known flavors such as vanilla, cinnamon, and few scents from flowers are extracted from aromatic compounds. Benzene with chemical formula C6H6 is a very common aromatic compound that contains six atoms of carbon held in the cyclic ring of alternate double bonds. It is also to be noted that not all aromatic compounds contain benzene ring. This can be explained by Huckel’s rule.