Arrange the Alkyl chlorides in the order of reactivity in SN1 reaction according to the data you obtained and compare it with theoretical order of reactivity. Are they the same? If not comment on why there is discrepancy.

Q: D. When the alkyl bromides (listed here) were subjected to hydrolysis in a mixture of ethanol and…

A: Answer: Characteristic reaction of alkyl halide is nucleophilic substitution that can take place…

Q: 9. The Friedel-Crafts alkylation of benzene often fails to provide only the mono-alkylated product…

A: Friedel-Crafts alkylation gives a mixture of mono and polyalkylated.

Q: Draw Sn1/E1 products of both reactions below or fill in the blank with appropriate stuffs for Sn1/E1

A: In both SN1 and E1 reactions, the first step is formation of stable tertiary carbocation. If the…

Q: do? 3) Predict the products of the following Friedel-Crafts reactions. a. b. OH H₂SO4 H₂SO4

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Q: Which SN1 reaction would you expect to occur more rapidly? Explain a. (CH3)3CC1+ H₂O → (CH3)3COH +…

A:

Q: Predict the product for the following Diels-Alder reaction. сосн,

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

Q: ii. Draw all the mono - bromo derivatives of X obtained by free radical bromination and determine…

A: The free radical bromination of molecule X results in mono-bromo products, where a hydrogen atom is…

Q: Rank the following radicals from least to most REACTIVE: PH2 CI *AsH2 Why did you choose this order?…

A: The solution is as follows:

Q: A student was about to turn in the products he had obtained from the reaction of HI with…

A: Markovnikov’s rule: unsymmetrical alkene reacts with hydrogen halide, halide ions goes to the more…

Q: Please explain why or why not the diene will or will not react with maleic anhydride.

A: The diene with the following are preferred- 4pi electron in conjugation, conjugated, less sterically…

Q: 4. Which alkyl halide would be most reactive in an SN1 reaction? Explain your answer. I Br IV Br Br…

A: The electrical effect is particularly important for the SN1 reaction. An SN1 reaction involves…

Q: How to complete this?

A: Acetylide anions are acting as strong bases and also strong nucleophiles due to sp3 hybridization on…

Q: Alec wanted to prepare to diene B to use in a subsequent Diels-Alder reaction. He thought he could…

A: (a) Requirement from question: FT-IR data We will take FT- IR of the compound and will compare the…

Q: Cannizzaro reaction has carried out using 3.1 mL benzaldehyde and strong base. What is the yield of…

A: The balanced equation is  2 C6H5CHO + KOH → C6H5CH2OH + C6H5COOK. here the reduction product is…

Q: This reaction also produces diacetylferrocene. However, this compound remains near the top of the…

A:

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: GENERAL SCHEME PDL2 R-X + R'B(OR),- R-R

A: This is scheme is example of suzuki reaction . In this crosss coupling reaction organohalide ( R-X)…

Q: Reagents Available a. Croz, H2SO4, H20 e. NABH4 b. На, Pd f. O3; then Zn, CH3CO2H c. KMNO4, H20 g.…

A: LiAlH4 used as reducing agent for carboxylic acid and pd/H2 used for reduction of double bond.

Q: Write contributing resonance structures to show how the negative charge in the intermediate in the…

A: The repositioning or the delocalization of lone pair of electrons or pi-bond electrons from one bond…

Q: explain why homolysis of the O-H bond in phenol requires considerably less energy than homolysis of…

A: a) O-H bond in phenol is more polar as compared to O-H bond in ethanol. This is because the…

Q: Ignoring isotope effects, after one E2 elimination with ethoxide, which bromine will predominate in…

A: The E2 elimination of alkyl halide forms an alkene from alkyl halide.  According to the…

Q: a. b. Cl₂ heat NBS light

A: Cl2 in presence of heat or light is used for chlorination reaction of alkanes. This reaction…

Q: 27. Explain why in this reaction an increase in temperature does not cause a different product to…

A: Resonance  occurs at high Temperature  due to which the Resulting Product is same as given Product.

Q: Arrange the following alkyl halides in order of immediate reactivity towards SN2 reaction. Assign 1…

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Q: 7. Please choose the two reagents below that you would use to synthesize molecule X via a…

A: Step 1:   Step 2: Step 3: Step 4:

Q: Section B (continued) В4. Answer all parts (i-iv). Explain the reactions and observations shown in…

A: P

Q: Part A 1. Explain why 1-bromo-2,2-dimethylpropane has difficulty undergoing both SÃ2 and SÃ1…

A: Sn1 reaction is unimolecular nucleophilic substitution reaction.Sn2 is bimolecular nucleophilic…

Q: 5. For the following compound rank the proton groups from most reactive to the least reactive in…

A: In the given molecule four types of carbon are present such as benzyl carbon, tertiary carbon,…

Q: Give the reagents that will yield the following transformation. NH₂ }– "OH Use the reagents provided…

A: We have to carry out the below given transformation.

Q: Select from the Table provided the reagent you would use to carry out each of the transformations…

A: The question is based on the concept of organic synthesis.We need to synthesize the product using…

Q: 5. Classify the following molecules in order of decreasing rate of SN2 reactions: Ethyl Chloride,…

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Q: (b) The activating and deactivating groups could affect the position(s) of the next incoming…

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Q: Which will react faster in SN2 displacement, 1-bromopentane or 2-bromopentane, and why?

A: The SN2 reaction is a substitution nucleophilic bimolecular reaction. In this reaction, bond…

Q: Which of the following is not true of SN₁ reactions? A. They are favored by nonpolar solvents. B.…

A: Here we are required to find the statement which is true for Unimolecular substitution reaction

Q: H A.

A: Diels-Alder reaction is a cyclic concerted cycloaddition reaction. These reactions in organic…

Q: 19. a. Label the reactive features, highlight the most reactive one, then highlight what it needs.…

A: Concept is based on cycloaddition reactions:   As per our guidelines we have to answer a,b,c only.

Q: What reagent system would work most efficiently in the transformation shown below a b i Selected…

A: The question is based on the concept of organic synthesis.  we need to synthesize the product using…

Q: 9. Diels-Alder(DA) reactions tend to be reversible. While some heat is needed to catalyze the…

A:

Q: What is the exact reaction mechanism behind this reaction? I understand how to get from BHA to the…

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.