1. еxcess CHa/K,COОЗ 2. Ag20, H20 3. Д 1. еxcess CH3|K,CОЗ 2. Ag20, H20 3. А CH;NCH,CH,CH,CH=CH, CH,=CHCH,CH=CH, 1,4-рentadiene ČH3 piperidine

Q: Like other electrophiles, carbocations add to alkenes to form new carbocations, which can then…

A:

Q: (a) Similar to alkanes, hydrogen gas can undergo radical bromination according to the reaction…

A: Energy released during bond formation and energy absorbed during bond cleavage

Q: Choose the right reagent or series of reagents from the ones listed to synthesize the following…

A: C6H6 and CH3CH2CH2COCl , AlCl3 followed by Zn(Hg) , HCl then NBS  Benzene is undergoing Friedel…

Q: Alkyl halides undergo elimination reactions to produce alkenes by the reacting with strong bases as…

A: The structure of cis- and trans- 1-Bromo-2-tertbutyl cyclohexane is given as:

Q: or SN2 Explain the order in which 1o (primary) alkyl halides reacted and explain why. The 1o…

A: The reactivity rate of SN2 reaction depends upon the concentration of both substrate and…

Q: Chlorination (halogenation) of 2-methylpentene will yield a final product of?

A:

Q: When we have discussed the enol-keto tautomerization of ketones in class, the isomerization has been…

A: During the keto-enol tautomerism, it is observed that the molecule prefers to stay in keto form when…

Q: Please state which is the main product when 2-methylbuta-1,3-diene reacts with one equivalent of HBr…

A:

Q: Write the complete and detailed mechanism for THREE EXAMPLES of SN1 reactions. In each example ,…

A: Number of functional group is associated with organic compounds which impart specific chemical and…

Q: The Wittig reaction can be used for the synthesis of conjugated dienes as the example below,…

A: The Wittig reaction is a usefull method for converting of aldehyde and ketone with a triphenyl…

Q: The reaction of 1-iodopropane with potassium thiocyanate (KSCN) in certain solvents results in the…

A: A. 1-Propene undergo addition reaction with H-SCN via carbocation formation. Due to greater +I and…

Q: From trans-1-chloro-2-isopropylcyclohexane, only 3-isopropylcyclohexene, the less substituted…

A: SOLUTION: Step 1: Treatment of trans-1-chloro-2-isopropyl cyclohexane with sodium methoxide in…

Q: A Moving to another question will save this response. Question 5 Which one of the following…

A: In the given compounds toluene,benzene, chlorobenzene,t-butyl benzene undergo a Friedel-crafts…

Q: NH₂ Br₂ AlBr3 HNO3/H₂SO4 OH NH₂ Br₂ AlBr3 NO2 HNO3/H₂SO4

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Q: This reaction usually give a mixture of cis- and trans-diphenylethene, but in this experiment, we…

A: In this question, first we will discuss about only trans isomers is prepared in this reaction. Then…

Q: One of the following Diels-Alder reactions will occur more rapidly than the other. Draw the major,…

A: The answer is as follows:

Q: The compound whose structure is shown here is acetyl acetone. It exists in two forms:the enol form…

A: (a)

Q: a. Label the reactive features of the following reactants, select the most reactive feature, then…

A: The organic reactions take place in more than one step with the help of reagents.

Q: The following compound can carry out the Diels-Alder reaction ,dilute the structure of the C4H6…

A: A problem based on spectroscopy, which is to be accomplished.

Q: C(CH3)3X +H20 C(CH3)3OH where (X-F, Cl, Br, I) give reaction with each of halogen as well determine…

A: An organic problem based on SN1 mechanism, which is to be accomplished.

Q: When carrying out this two step procedure (bromination and subsequent elimination) on cyclopentene,…

A: The product of given reaction surely could not be alkyne since it is strained one.

Q: Predict the predicted product of the reaction shown in the following diagram:

A: -NH2 group is strong ring aactivation group, hence when amino benzene (aniline) is treated with…

Q: For SN2 Explain the order in which 2o (secondary) alkyl halides reacted and explain why. 2o…

A: The type of nucleophilic substitution reaction taking place between a secondary alkyl halide and a…

Q: Among a primary, secondary, or tertiary carbocation, which is least favored for SN2 reactions?…

A:

Q: Organometallic reagents are useful synthetically because they react as if they :: that is, carbon…

A: Organometallic substances are organic compounds having negatively charged organic part and…

Q: What would be the order from fastest to slowest if dichloromethane added to these compounds reacted…

A: As the electron density on the ring increases polarising power of ring to the bromine will also…

Q: a. Label the reactive features, highlight the most reactive one, then highlight what it needs. Also,…

A: Hydroboration reaction

Q: Step 4: You have determined that one of the precursors is a vinyl halide, while the other is a vinyl…

A: Soln

Q: OH POcl3 DLIAI H4, 2) H3 O* CI Alcl3 Pyridine cl cl HCl Alcls

A: The synthesis process in above picture is correct.  Upon reaction of secondary/tertiary alcohol with…

Q: An isomer of tetramethylbenzene undergoes nitration to yield a single product. Based on this…

A: An isomer of tetramethyl benzene undergoes nitration to yield a single product. Based on this…

Q: Suggest an experimental procedure whereby this protecting group can be removed to regenerate the…

A:

Q: The halogenation of 2-but he with 1Cl2 will lead to what major product?

A: The halogenation of 2- butene with Cl2 will give 2,3 dichlorobutane as major product.

Q: The scheme below shows two reactions starting from compound Z. Heating Z results in a loss of CO, to…

A:

Q: When piperidine undergoes the series of reactions shown here, 1,4-pentadiene is obtained as the…

A: Please find below the methyl-substituted piperidine which forms 1,5-hexadiene, and 1,4-pentadiene…

Q: addition of hbr to a double bond with an ether (-or) substituent occurs regiospecifically to give a…

A: Addition of HBr to the double bond gives electrophilic addition reaction. During this reaction, a…

Q: a. Label the reactive features of the following reactants, select the most reactive feature, then…

A:

Q: Among a primary, secondary, or tertiary carbocation, which is most favored for SN1 reactions?…

A: Among a primary, secondary or tertiary carbocation which is most favored for SN1 reactions? Explain…

Q: BS21008 Organic Chemistry for the Life Sciences Assignment Week 7 Bearing in mind Huckel's rule,…

A:

Q: Indane can undergo free-radical chlorination at any of the alkyl positions onthe aliphatic ring.…

A: Indane is an organic compound which two part, one part is an aromatic ring and other part of the…

Q: Which of the following is (are) the most likely reaction product(s) in the monobromination of…

A: The above reaction can be explained as:…

Q: b) Support your answer with the appropriate energy diagrams. (Energy diagram should show two…

A:

Q: For SN1 Explain the order in which 2o (secondary) alkyl halides reacted (fastest to slowest) and…

A: The rate of the SN1 reactions depends upon the concentration of alkyl halide only. This kind of…

Q: Like other electrophiles, carbocations add to alkenes to form new carbocations, which can then…

A: Analysis of the provided reaction shows that nerol is starting compoundin both the reactions . The…

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.