Rank the alkenes in order of increasing Amax for the to n transition in the UV spectrum. (shortest wavelength B A

Q: Draw the two possible products formed when this diene reacts with HBr. Do not include any byproducts…

A: When a conjugated diene i.e. alternate double bond molecules is treated with HBr, there is a…

Q: HEMISTRY AT TETRAHEDRAL CENTERS cis-1,2-Dimethylcyclohexane is optically inactive even though it has…

A: Presence of chiral carbon centre is not the only requisite for a molecule to be optically active.…

Q: Draw the kinetic and the thermodynamic addition products formed when one equivalent of HBr reacts…

A: The stability of carbocation decides the formation of the kinetic product whereas the stability of…

Q: 2,4-hexadiene Cis H Cis B) Draw the HOMO (highest occupied) contributing the Stereospecific…

A:

Q: Assign E or Z stereochemistry to the following compound (red = 0): %3D

A: The stereoisomers are the isomers that have the same molecular formula but a different spatial…

Q: 1 2 3 4 5

A: Highly substituted alkene is more stable.If alkenes are equally substituted then alkene containing…

Q: 7) Predict the major product HBr 40°℃

A: Given is organic reaction.The given reaction is hydrobromination reaction.The given starting…

Q: Describe stereoselective, regioselective, or chemoselective, the reactions below.

A: In case one we write the most stable structure in chair form, now their is two possibility to attack…

Q: Which of the following describes the sigmatropic rearrangement that occurs in the reaction shown…

A: Option E is the correct answer.[1, 5] Sigmatropic Rearrangement.Explanation:Step 1: reaction…

Q: What is the stereoelectronic requirement for this reaction? (three correct answers) Br KOME A KBr +…

A: The question is asking about the stereoelectronic requirements for a reaction involving a bromide…

Q: Identify the expected major product of the following Diels-Alder reaction. OI O II O III O IV OV +…

A: Diels Alder reaction requires a diene and a dienophile. The diene must remain in cis position. And…

Q: Determine the structure from the following name: (2S,4R)-4-bromo-2-hydroxycyclohexan-1-one

A:

Q: Rank the following alkenes in order of increasing stability: Select one: a. <l<V<l<N b. N<ll<ll<l…

A: The stability of alkenes is primarily determined by their degree of substitution and the presence of…

Q: 56. What is the major product? (A) (C) -Br -Br (NBS) Br N (D) =0 ROOR, hv (B) Br -Br -Br

A: The given reaction is an example of bromination reaction of cyclopentene to give corresponding allyl…

Q: a) I b) II c) III d) IV e) V I WHICH DIENE IS MOST STABLE: is tes W II III IV V

A: The objective is to determine the most stable diene.The diene is the molecule having the two double…

Q: As shown below, when compound 6a is heated, (1Z, 3Z)cycloheptadiene is formed. When the related…

A: Both given reactions are 4 Pi electrons i.e. in the presence of heat the change their…

Q: ОН сон O₂N HO3S N2 N₂ Product(s) Product(s)

A: An organic chemical reactions in which the diazonium cation (R-N2+) reacts with another aromatic…

Q: Which of the alkenes shown below can't be assigned as an E or Z isomer? O b, c, e Oa, c, e Oa, c, d…

A: The E-Z system of nomenclature is used the represent the arrangement of groups around a C-C double…

Q: 6. Propose a mechanism (curved arrows) for the following SN 1 reaction. Based on the mechanism, do…

A: It undergo via carbocation intermediate. It forms racemic mixture

Q: Arrange these alkenes in order of increasing stability (least stable first). B&B 2 1 1, 2, 3 O2, 3,…

A: Given are organic compounds.The given compounds are alkenes.Order of stability of…

Q: : Br-CH₂-CH3 + 30-H

A: A chemical reaction

Q: 3. By what mechanism is the following reaction likely to occur? a) SN1 b) SN2 c) E1 d) E2 e)…

A:

Q: Give me mechanism. Please explain each step!

A: Following is the polymerization reaction of the given alkene.

Q: > Identify ALL compounds DO NOT undergo highly favorable rearrangements a different carbocation…

A: If after rearrangement stable, carbocation is formed then only rearrangement will take place. If a…

Q: Rank the following carbocations in terms of stability from lowest to highest. to A B C D

A:

Q: Predict the major product(s) of the following reaction. HBr Br **** Br Br Br IV Multiple Choice Only…

A: The reaction given is,

Q: F 11 ד

A: Diels-Alder reaction: It is a [4+2] cycloaddition reaction between a diene and dienophile to form a…

Q: Four alkenes (A-D) are shown below. Arrange the letters to represent the order of alkene stability…

A: • Stability of alkene is directly proportional to number of alpha hydrogens. Also more substituted…

Q: Rank the molecules A to D shown below by decreasing reactivity towards iodo cyclohexane. H;C-CH,OH…

A: Correct option is 2 . B &gt; A &gt; C &gt; D. B trifluoro ethanol is more acidic means more reactive…

Q: Which of the following dienes is the most stable? (A) (B) (C) (D) Compound D Compound A Compound C…

A: Types of diene based on the position of double bond and stability of diene

Q: 9. Which of the alkyl halides shown will undergo the fastest SN2 reaction?

A: The bimolecular nucleophilic substitution reaction is a concerted reaction that occurs in a single…

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.