(2) Which is the most reactive substrate in the electrophilic addition? ( A. CH3-C=CH2 B. CH3-C=CH-CH3 C. H3CH2C-CH=CH2 D. CH3-C C-CH3 CH3CH3 ČH3 ČH3

Q: Classify following solvent as protic or aprotic                 CH3NO2

A: Protic solvents are those which contain protons bonded with high electronegative atoms like oxygen…

Q: If you lost a double bond but gained a cyclic ring what would you see in IR?

A: A question about IR spectrum, which is to be accomplished.

Q: DMSO 0

A:

Q: 4. Are there any RX compounds from part A that are not expected to undergo an Sn1 or SN2 reaction?…

A: Note: Chloro benzene, bromo benzene cannot participate in sn1 or sn2 due to unstable carbocation and…

Q: 2. Explain why tert-butyl chloride will undergo an Sw1 but not an Sw2 reaction process?

A:

Q: Which solvent would have a higher reaction rate for SN1? acetone ethanol Why does the solvent you…

A: Ethanol is a polar solvent that is used in SN1 reactions.

Q: Classify following solvent as protic or aprotic                CH2Cl2

A: Protic solvents are solvents which contains protons bonded with high electronegative oxygen and…

Q: Draw the structure(s) of the major organic product(s) obtained after workup of the following…

A: The given reactant is an ester and a secondary amine.

Q: Explain how heteroduplex formation is resolved during transformation?

A: We have find out heteroduplex formation is resolved during transformation.

Q: Why does the carbomethoxy group directs the reaction to positions that are meta to it ? b) Why the…

A: Hi there! Since you have posted multiple subparts, we will answer the first 3 subparts for you. Part…

Q: Explain why compound A is much more stable than compound B.

A:

Q: 1) How will you describe whether any compound has been oxidized or reduced? Support your answer with…

A: Note: As per our guidelines, we are supposed to answer only one question. For other question to be…

Q: Resveratrol is an antioxidant found in the skin of red grapes. Its anticancer, anti-inammatory, and…

A: a). Resonance structures for the radical that results from homolysis of the OH bond: The radical…

Q: ctured, You need your final alcohol products D a

A: Secondary alcohols can be produced by the organolithium reaction with aldehyde.

Q: The carbocation electrophile in a Friedel-Crafts reaction can be generated in ways other than by…

A:

Q: Define a two-step method consisting of Grignard addition followedby dehydration, or a one-step…

A: Grignard reagent is an organomagnesium reagent which is used to introduce alkyl groups at carbonyl…

Q: Explain the E2 mechanism (bimolecular elimination) of of Elimination ?

A:

Q: For the given below ee values, calculate the percentage of each enantiomer present.         60% ee

A: Constitutional isomers can be defined as the molecules which have the same molecular formula and…

Q: Axial alcohols are oxidized faster than equatorial alcohols by PCC and other Cr6+ oxidants. Which OH…

A: a) The 3-D representation of the given compound is: Since the OH group represented by ‘a’ is on…

Q: (a) Draw the arrow-pushing mechanism between isoprene and MVK that leads to the major regioisomer…

A: a) The mechanism of the reaction that leads to the formation of major product is as follows:

Q: In some nucleophilic substitutions under SN1 conditions, complete racemization does not occur and a…

A: a.

Q: In both SN1 and SN2 tests, why should 2-chlorobutane react more slowly than 2-bromobutane?

A: We are authorised to solve only one question at a time. Please post rest of the questions…

Q: Which position(s) on the ring will be most likely to be sulfonated? Explain your reasoning for…

A: In the sulfonation Reaction, we can used sulfonating agent like SO3, py or SO3 / H2SO4. This reagent…

Q: Explain how substituents on thearomatic ring promote substitutionat some positions but not at others

A: Two types of groups can be present on aromatic ring  a) electron donating groups like -NH2, -OH, -OR…

Q: (b) What are oxidative addition and reductive elimination steps in a catalytic eycle?

A: 1. Oxidative addition is a process that increases both the oxidation state and coordination number…

Q: а. arbousto CH3 abnuoginod. С. b.

A: Rule of IUPAC- 1) Longest chain as parent chain. 2) Numbering start from those side where more prior…

Q: Why is alkoxide (RO-) a stronger base than Chloride? Why are alcohols typically poor electrophiles?

A: 1. alkoxide ions are better proton acceptors as compared to hydroxide ion which makes them stronger…

Q: For the following pair of carbocations (A and B), select the one that is more stable and explain…

A:

Q: Draw the structure of the major product of 2-methyl-3-heptyne + H2, Lindlar catalyst f.benzene +…

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Q: BuLi -Br Ph3P A В + ↑

A: This reaction is Wittig reaction. Alkene is produced from carbonyl group.

Q: Account for the fact that tetrahydrofuran (THF) is very soluble in water, whereas the solubility of…

A: Ethers are polar molecules in which Oxygen bears a partial negative charge and each attached to…

Q: Determine the absolute Configuration (Rors) of the Stereogenic centre in compounds (i) and (ii)

A:

Q: 1. Which alkene is the major product of this dehydration?

A:

Q: 4 och 5 är OCH3 4

A: Nucleophiles are electron rich species and they always show tendency to attack the electron…

Q: Select the member of each pair that shows the greater rate of SN2 reaction with KN3 in acetone.

A: SN2 reaction rate depends upon the steric effect. Higher the steric hindrance, lower would be the…

Q: SN1 is always a competing reaction of E1. True or False?

A: SN1 Reaction: A tertiary alkyl halide substitutes nucleophile by the removal of halogen as leaving…

Q: Which pair(s) can be separated by chemically active extraction? |-CH3CH2NH2 and C,H5NH2…

A: The pairs of organic compounds given are I. CH3CH2NH2 and C6H5NH2 II. (CH3CH2)3N and CH3CH2NH2  III.…

Q: A mixture contains equal amounts of compounds A–D. a.Which compounds alone are optically active? b.…

A: a. Optical active compounds are those where non-superimposable images are formed. They have a chiral…

Q: 2. Reactivity of Aldehydes and Ketones a. Rank the following aldehydes and ketones in order from…

A: Given: Aldehydes and ketones : A, B, C, & D. The increasing order of reactivity is as follows:

Q: Which group in following pair is assigned the higher priority? −CH2Br, −CH2CH2Br?

A: In R, S nomenclature, the atom or the group which has highest atomic number.

Q: In the preparation of para-iodo nitrobenzene,   a)If instead of KI, CuCl was added in the…

A:

Q: Select the member of each pair that shows the greater rate of SN2 reaction with KN; in acetone. Set…

A: The nucleophilic substitution reaction of the leaving group (which usually consists of halide groups…

Q: 4. Are there any RX compounds from part A that are not expected to undergo an SN1 or Sn2 reaction?…

A: Note: primary alkyl halides prefers sn2 reaction. secondary alkyl halides prefers sn1 or sn2 depends…

Q: PCY3 CI Ru Ph PCY3

A: Metathesis reactions are chemical reactions in which two hydrocarbons (alkanes, alkenes or alkynes)…

Q: Part A: In the attached figure, rank the following compounds in order of their expected reactivity…

A: Compounds that has good leaving group more likely undergoes substitution reaction.

Q: B D Write the letters that correspond to the starting material and the product for the mechanistic…

A: In this question, you give the letters for starting material and Product ( on the right side energy…

Alkanes and Cycloalkanes

Alkanes are saturated organic compounds which are made up of C and H atoms. Alkanes have the general formula of CnH2n+2. Alkane contains sp3 hybridized carbon atoms with four sigmas (σ) bonds & every hydrogen atom is connected with one of the carbon atoms. The size of the alkane could be determined by the number of carbon atoms located in it.