Synthesis F Please Include the reagent and intermediate as well as the Meta direction OH acyclic starting materials containing 4 or fewer C atoms H3C (+/-) Desired Product H

Q: Synthethic

A: 1- EtOH, H+ ( Formation of ester bond ) 2- H2, Pd(C) [ removing of protecting group )  3- K2Cr2O7,…

Q: Make a SynthesiS Starting S HCECH + materials w l'Carbon and any necessary reagents

A: The synthesis route for preparation of 2,6-octadiene is given by

Q: Draw the organic product of the following reaction. Select Draw Ring H CI CH;CH,C=CCH, CH, + 2Cl, →

A: The addition of Cl2 to an alkyne is analogous to adding Cl2 to an alkene. The π electrons, from the…

Q: Consider the reaction below to answer the following question(s): or 'Н ini H H NaOEt EtOH + H₂O…

A: Internal aldol condensations can occur in compounds containing two carbonyl groups in which atleast…

Q: Identify a more stable tautomer from the following enol and keto tautomers. Explainyour answer…

A: Phenol is an aromatic Organic compound, with Molecular formula of C6H5OH. It exist as first aromatic…

Q: .CI Draw the major organic product(s) if the compound is reactive. Assume that conditions are…

A: Applying concept of fredalcraft alkylation reaction.

Q: raw a stepwise mechanism for the following reaction: Br CH3CH2OH

A: This given reaction is based on williamson ether synthesis. This reaction proceeds via SN2 path.…

Q: b) Use curved arrow formalism to draw the mechanism of the reaction shown in a). product(s) Brz…

A: ->First of all alkene reacts with Br2 and cyclobromonium ion is formed because there is present…

Q: 46. The indicated bond is: of H,C CI A) Nucleophilic because it is electron-deficient. B)…

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Q: Br2 CH3OH

A: Organic reaction mechanisms

Q: POCH3 O A curved reaction arrow would start from the O in "OCH3. O A curved reaction arrow would…

A:

Q: For each reaction, draw the complete mechanism and the major organic product(s), paying attention to…

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Q: 2. Draw the mechanism for the given reaction For "Excellent", draw all possible products including…

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Q: 5) which is better electrophile, the moot reactive upon rucleophilic attack + best reaso'n? OR CI )…

A: The Carbon atom of carbonly group (-C=O) in aldehydes, keotnes and acid derivatives acquires partial…

Q: CI AICI3

A: Hh

Q: Sometimes carbocation rearrangements can change the size of a ring. Draw a stepwise, detailed…

A: The -OH group of alcohol abstracts a proton (from acid) as shown below:

Q: Draw the major product of this reaction. Ignore inorganic byproducts. CI excess NH3 Select to Draw

A: Answer: Given reactant is an acid chloride derivative which is reacting with a nucleophile ammonia…

Q: draw the major product of the following reaction, and then the arrow-pushing mechanism: H* CH3…

A: The major product of the reaction is

Q: 9. Draw mechanism for all the substitution and elimination products for the following reaction.…

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Q: CI NaSCH3 18. Be *very specific* about the stereochemistry of the product(s) of this reaction

A: Since you have posted multiple questions, we are entitled to answer the first only.

Q: A carbocation is a good a) electrophile b) nucleophile c) neither O a O b

A: In this question, we will see that the carbocation is a good Electrophile or Nucleophile.  You can…

Q: Cve a Synthesis mechanism the fattowing ompuund focom hydrrocorbons कल् Cककनक ला चामल बा n any…

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Q: What are the possible constitutional isomers and rank by SN2 reaction.

A: Isomers are the compounds having same molecular formula but different structure. The phenomenon…

Q: A. Draw the acceptable major product for the following reaction H,SO4 Н-ОН Н-ОН H* H,0 H,SO4 H,O

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Q: CHs CH HCI

A:

Q: Br. Br

A: Strong nucleophile ----->  SN2 mechanism Weak nucleophile -------> SN1 mechanism Less degree…

Q: Br OOCH3

A: Reaction 1: Secondary alkyl bromide and strong base (methoxide ion) prefers E2 elimination. Reaction…

Q: j. 1,2-epoxybutane + acid in methanol Reaction Type(s) Mechanism(s) Product(s)_ Stereochemistry (if…

A: Answer-1  Reaction Type - Epoxide Opening in Acidic Condition  Answer-2  Reaction Type- Acid Base

Q: prese Maxwell Draw the major organic product of the reaction shown. Select Draw Rings More HI H3C-OH

A: in nucleophilic substitution reaction nucleophile attacks on substrate and forms product.

Q: alkene that, upon ozonolysis reaction, gives only H. H' Select one:

A: In this question we will Identify the starting material Alkene which give di-aldehyde Product.  You…

Q: Identify F in the following reaction sequence. F was converted in several steps to the…

A: The entire mechanism of the reaction is as follows:

Q: Draw the product of attached reaction

A: Organometallic compounds are used to increase the carbon number in the molecule. Organolithium…

Q: Draw the curved arrow mechanism for the following reaction: Ph- Но- НО ÓMe CH2CI2 -78 °C 1 h TMEDA…

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Q: 24. For the following acid-base reaction draw the correct curved arrow mechanism; CH3-CH2-CH2-CH-SH…

A: We have to draw arrow mechanism .

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

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Q: 1.70 An a,ß-unsaturated ketone reacts with a conjugated Wittig reagent to produce a relatively…

A: The wittig reaction is a chemical reaction for the formation of alkene from aldehyde or ketone with…

Q: alkyl halde The mechanism of this reaction is SN (SN2 or Sy1?). Explanation: Jvcleophile

A: SN2 reactions occur in a single step whereas SN1 reactions are those that occur in 2 steps. SN2…

Q: Draw the curved arrows to show how the product is formed. :ö: :0: :0

A: ⊙Electron density flow hight to low region.so     arrow start from higher e- density geos to…

Q: Draw the most likely products of each reaction. d. Predict which reaction will be faster. e. Draw an…

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Q: Draw all products, including stereoisomers, in attached reaction.

A: Stereoisomers are isomers that differ in the spatial arrangement of atoms in a three-dimensional…

Q: Draw the neutral organic product when butanone reacts with one equivalent of ethanol in acidic…

A: 1. According to organic chemistry,  species or group having electrons richness are known as…

Q: Choose the correct product(s) for the following reaction:

A: Benzene undergo electrophilic substitution reactions If electron withdrawing group is present on…

Q: CH3ONA in CH3OH ОН

A: The reaction starts with the attack of CH3O- to the C-O bond of ether to form a new ether bond and…

Q: synthesis reaction(s)

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Q: Draw the products of attached reaction, indicating the stereochemistry around any stereogenic…

A: This reaction follows SN1 mechanism. In SN1 mechanism firstly leaving group leaves and carbocation…

Q: NH Ci

A: The basic Hydrolysis of Carboxylic acid derivatives give their respective Carboxylic acids with some…

Q: Draw the major organic product for the reaction shown. NH LIAIHA

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Q: Draw the major organic Product of shis real seveuchemical of he producto. If reachon is slow or will…

A: The given reaction will take place. Since the alkyl halide used is secondary alkyl halide and the…

Q: Draw the major product(s) for reaction of methyl pentanoate with: LIAIH4; then H30*

A: Ester on reduction with strong reducing agent LiAlH4 followed by acidification gives primary…

Q: Draw the equilibrium chair confirmation of cis1-chloro-3-methylcyclohexane. Interpret the E2…

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Ionic Equilibrium

Chemical equilibrium and ionic equilibrium are two major concepts in chemistry. Ionic equilibrium deals with the equilibrium involved in an ionization process while chemical equilibrium deals with the equilibrium during a chemical change. Ionic equilibrium is established between the ions and unionized species in a system. Understanding the concept of ionic equilibrium is very important to answer the questions related to certain chemical reactions in chemistry.

Arrhenius Acid

Arrhenius acid act as a good electrolyte as it dissociates to its respective ions in the aqueous solutions. Keeping it similar to the general acid properties, Arrhenius acid also neutralizes bases and turns litmus paper into red. 

Bronsted Lowry Base In Inorganic Chemistry

Bronsted-Lowry base in inorganic chemistry is any chemical substance that can accept a proton from the other chemical substance it is reacting with.