Rank the relative rates of the alkyl halides in an SN 1 reaction. CH3 Fastest SN 1 reaction Slowest SN 1 reaction Answer Bank CH3 Br Br CH3 H3C-Br -Br CH3 CH3

Q: Rank the following in order of reactivity in an E1 reaction, (1 = most reactive in an E1 reaction; 3…

A: Elimination reaction of alkyl halide: Alkyl halide gives an elimination reaction by reacting with a…

Q: Rank the relative rates of the alkyl halides in an SN1 reaction. H3C-1 CH3 CH3 CH₂ H₂C Fastest SN 1…

A: SN1 reaction means unimolecular nucleophilic substitution reaction.  The reaction proceeds in two…

Q: Decide the mechanism for each reaction and predict the MAJOR product. a. b. j CN HO Br CN NaCN CHCN…

A: Product of following reaction can be made by applying appropriate reaction mechanism.

Q: XIV. Identify the reagents a and b in the following scheme. a Br b

A: First reaction is allyl bromination, which is smoothly done by N-bromosuccinamide in presence of…

Q: Which Diels Alder reaction will go best (fastest, best yield, lowest temperature)? CH₂ FCH₂ CH₂ CH₂…

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Q: Which reaction would proceed with the fastest rate? Why? OH OH NaBr HBr top reaction; better…

A: The substitution reaction in which elimination of leaving group and the attack of nucleophile takes…

Q: Br. Br NaOCH3 DMF

A: SN2 reactionIt is a bimolecular nucleophilic substitution reaction in which the rate of reaction is…

Q: the boxes with the appropriate product of each reaction. Be sure to watch your stereochemistry! Br…

A: An organic compound can be converted to another compound byreacting with another compound or…

Q: Predict the Robinson annulation product. NaOH H H20 heat

A: Robinson annulation is an intramolecular Aldol condensation for the ring formation.

Q: Sy1 A -Br + Br Syl -Br Br -Br Br +

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Q: Draw the major and minor monobromination products of this reaction. NBS hv Q

A: NBS is actually N-bromosuccinimide and given reaction is the characteristic reaction of alkene in…

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

A: The formation of carbocation is shown below.

Q: Draw the transition state for each reaction.

A: Please find below the transition state of reaction 1.

Q: What is the major product of the following reaction? Br2 ? FeBr3

A: The objective of the question is to find the major product of the given reaction in which Br2/FeBr3…

Q: Arrange the reactants from fastest to slowest in an S№2 reaction. (CH3)2C(CI)CH3 CH3CH(CI)CH2CH3…

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Q: Draw the starting material that would be needed to make this product through a Dieckmann reaction. о…

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Q: Circle the carbonyl addition that occurs at a faster rate.

A: We have to find the carbonyl addition from the given set of reactions which occurs at a faster rate.

Q: Hi there! Can you help me complete this reaction with the reagents and type name. Thanks! d) OCH3…

A: The given equation is we have to find the reagent used and type of chemical reaction.. Here, the…

Q: Which is faster in Sn1 reaction?

A: In SN1 reaction, at first a carbocation is formed when the leaving group departs. Then a nucleophile…

Q: Draw the products of each nucleophilic substitution reaction. CN Br a. (CH3)3C- b. (CH3)3C- acetone…

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Q: In each reaction box, place the best reagent and conditions from the list. 1) 2) Answer Bank H₂O₂…

A: The objective of the question is to find the best reagent and conditions for the given conversion.A…

Q: Circle the best nucleophile in ammonia: NaCl, NaOH, NaCH3, Nal Circle the best nucleophile in…

A: We have to find the best type of nucleophile in ammonia and acetone

Q: R OR1 -R2 R R-CEN

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Q: Draw the major monochlorination product of this reaction.

A: Given is organic reaction. The given starting compound is alkane.The given reaction is photochemical…

Q: What is the first step in an SN1 reaction? Group of answer choices Attack of the nucleophile. Loss…

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Q: What alkenes are formed from each alkyl halide by an E1 reaction? Use the Zaitsev rule to predict…

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Q: In an Sn2 reaction which one of these would be the poorest leaving group

A: Option 2 should be the correct answer Good leaving groups are the weak bases which tend to leave…

Q: Choose the reagent(s) that would be most likely to complete this reaction. 1. Hg(OAc)2, H₂O 2.…

A: We have been given an organic reaction and we have been asked to choose correct option from given…

Q: Br NaOEt EtOH c.

A: Given substrate is 1-bromo-1-phenyl-2-methyl butane.NaOEt will use as a base and EtOH is solvent…

Q: Choose the reaction that involves a carbocation intermediate: Br REACTION A: NH2 REACTION B: OH CI…

A: The intermediates formed for the mentioned reactions depends on the pathway which are followed by…

Q: Br CH3 CH3 CH3OH heat CH3 CH3

A: E1 elimination reaction follows through formation of carbocation intermediate.

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.