CI CI + CO2 + NaCI O Na CI CI sodium trichloroacetate

Q: Devise a synthesis of each alkene using a Wittig reaction to form the double bond. You may use…

A: Given target compounds,

Q: Draw a stepwise mechanism for the conversion of dihalide A and cyclohexane-1,4-diol to polyether B…

A: Since AlCl3 is a Lewis acid and hence it will extract Cl from the compound A forming a carbocation…

Q: Prepare each compound from cyclopentanol. More than one step may be needed.

A: Organic synthesis processes are used to prepare different organic compounds by organic reactions…

Q: Draw the organic products formed when attached allylic alcohol A is treated with following reagent.…

A:

Q: Synthesize each compound from toluene and any other organic or inorganic reagents. a. CsHsCH2Br b.…

A: Synthesis of the targeted compound can be done in different ways. But, here I am showing the most…

Q: Draw the products formed when each compound is treated with HNO3 and H2SO4.

A: EXPLANATION: a) part -OCH3 is ortho, para director whereas -COOCH3 is a meta director.Because -OCH3…

Q: Draw the product and indicate the stereochemistry when the given alcohol is treated with each…

A: Hello. Since your question has multiple sub-parts, we will solve the first three sub-parts for you.…

Q: Devise a synthesis of each compound from benzene. You may use alcohols with one or two carbons and…

A: This reaction is the conversion of Benzene to ortho-bromoacetanilide.

Q: draw

A: We will write the reaction

Q: Synthesize each compound from cyclohexanone and organic halides having s4 C's. You may use any other…

A: a)

Q: Prepare 1-nonen-3-ol from heptanal and acetyle a. CH3(CH2)5CH(OH)-CH=CH2

A: Given is synthesis reaction.

Q: When bromoethane is refluxed with KOH in an alcoholic medium, compound Y is formed. Give the…

A: Alkyl halides on heating with  alcoholic KOH undergoes dehydrohalogenation and an alkene will be…

Q: Show how to convert propene to each of these compounds, using any inorganic reagents as necessary.…

A: Since you have asked question with multiple subparts, we will solve the first 3 subparts for you, If…

Q: Give the structure corresponding to each IUPAC name. a. 2-methoxypropane b. cyclobutyl ethyl ether…

A: Since you have posted multiple sub-parts, the answer for first three sub-parts are given below.…

Q: Convert each compound to its enol or keto tautomer. HO- a. b. CH CH3

A: The given compounds has to be converted into keto or enol form.

Q: What product is formed when p-dimethylbenzene (also called p-xylene) is treated with each reagent?

A: In the given electrophilic substitution reactions of p-dimethylbenzene, electrophile substitutes the…

Q: CI (d) CH3-CH=CH-CH3 CH3-CH2-C-CH3 CI

A:

Q: Draw the products formed when (CH3)2C=CH2 is treated with each reagent.a. HBrb. H2OH2SO4c. CH3CH2OH,…

A: Markovnikov’s rule:Negative part of the addendum goes to the carbon atom having less number of…

Q: Choose the major product when 2-bromo-2-methylpentane is treated with sodium ethoxide in ethanol…

A: In the reaction 2-bromo-2-methylpentane is treated with sodium ethoxide in ethanol to form the…

Q: Alkene is converted to alkyl halide by reaction with HCl . (T/F) Iodoform is used as an antiseptic.…

A: NOTE ; Since you have posted multiple sub-parts,we'll solve only first three sub-parts for you.To…

Q: Prepare each compound from cyclopentanol. More than one step may beneeded.

A: (a) The reaction of alcohol with HCl in the presence of catalyst ZnCl2 leads to formation of alkly…

Q: 1-Chlorobutane is treated first with sodium acetylide, then sodium hydride, then methyl iodide, and…

A: We have given that  1-Chlorobutane is treated first with sodium acetylide then sodium hydride then…

Q: CH2N2 Et,0 HO2C MeO2C HO2C A HO2C C D

A: When a carboxylic acid react with Diazomethane then methyl ester is formed as the major product.…

Q: Draw the structure of a hydrocarbon that reacts with 2 equivalents of H2 on catalytic hydrogenation…

A:

Q: N-Chlorosuccinimide (NCS) serves as a source of Cl+ in electrophilic addition reactions to alkenes…

A: Since alkyne is a nucleophile. hence the Cl+ produced by the N-Chlorosuccinimide will be attacked by…

Q: H₂C a b d e H3C Provide the missing reagents (a, c, e) and intermediate products (b, d) formed as…

A: This is multi step synthesis so everyone has own thinking and he can used different reagent for this…

Q: Draw a stepwise mechanism for the conversion of dihalide A and cyclohexane-1,4-diol to polyether B…

A:

Q: Show the arrow pushing mechanism using the reagents (1) Pd/C, H2 (2) H2SO4

A: The Mechanism for the following reaction is - First step - hydrogenation in presence of Pd/C Second…

Q: In addition to using CHX3 and base to synthesize dihalocarbenes, dichlorocarbene (:CCl2) can be…

A:

Q: Dehydration of 1,2,2-trimethylcyclohexanol with H2SO4 affords 1-tert-butylcyclopentene as a minor…

A: a) The stepwise mechanism that describes the formation of 1-tert-butylcyclopentene is as follows,…

Q: Synthesize each compound from benzene.

A: Note: According to Q&A rules I am answering the first sub-part only. Please repost the remaining…

Q: Draw the organic products formed when cyclopentene is treated withfollowing reagent.  CH3CO3H

A: The organic reactions help in the conversion of one organic compound into another compound. This…

Q: Synthesize each compound from toluene (C6H5CH3) and any other organic or inorganic reagents.

A: A.

Q: What is the structure of cis-jasmone, a natural product isolated from jasmine owers, formed by…

A: Lindlar catalyst: The catalyst is used for the hydrogenation of alkenes in a syn manner. This means…

Q: Draw a stepwise mechanism for the conversion of dihalide A andcyclohexane-1,4-diol to polyether B in…

A: The stepwise mechanism is given below -

Q: Draw the products formed when D-altrose is treated with each reagent. a. (CH3)2CHOH, HCl b. NaBH4,…

A: Hi, since there are multiple sub-parts posted we will provide you with answers for the first four…

Q: Draw the product and indicate the stereochemistry when the given alcohol is treated with each…

A: Given, a.

Q: Reaction of alcohol below will give an ether as the product. Select the CORRECT IUPAC nomenclature…

A: For IUPAC naming select the longest hydrocarbon chain containing functional groups and substituents…

Q: Draw the major organic product formed by reaction of 2-hexyne with the following reagent: H2/…

A: Given :-  2-hexyne + H2/Lindlar catalyst →  To determine :-  major product formed in the given…

Q: When bromoethane is refluxed with KOH in an alcoholic medium, compound Y is formedl. Give the…

A: Solution:- It is asked about reaction of bromoethane is refluxed with alcoholic KOH. KOH is a strong…

Q: Draw the products formed when (CH3)2C=CH2 is treated with following reagent. Br2, H2O

A: The reaction is as follows:

Q: Reduction of Acetic acid with Lithium aluminium hydride gives ethyl alcohol. (T/F)

A: Given: Reaction of acetic acid with LiAlH4

Q: Ketone A can be converted to alkene B in a one-step reaction via route I. It can also be converted…

A:

Q: Draw the products formed when each alkene is treated with O3 followed by Zn, H2O.

A: The reaction of an alkene with O3 followed by Zn in the presence of H2O is known as ozonolysis…

Q: Synthesize each compound from cyclohexanol, ethanol, and any other needed reagents.

A: Since you have posted a question with multiple sub-parts, we will solve first three subparts for…

Q: Devise a synthesis of each compound using CH3CH2CH=CH2 as the starting material. You may use any…

A:

Q: Devise a synthesis of each compound from benzene. You may use alcohols with one or two carbons and…

A: In this question, we will synthesized the given products from the given starting materials benzene.…

Q: (a) What reaction conditions are needed to convert (R)-2-ethyl-2-methyloxirane to…

A: (a)Reaction of (R)-2-ethyl-2-methyloxirane converted to (R)-2-methylbutane-1,2-diol:

Q: H3C a C e H3C CH2NH2 Provide the missing reagents (a, c, e) and intermediate products (b, d) formed…

A: Here we are required to find the reagent to carry out the synthesis.