Q: 3. Circle the best substrate for a nucleophilic substitution reaction. HO. OCH, SH
A: In a nucleophile substitution reaction, the rate of the reaction depends on the nucleophilicity of…
Q: Show which compound can act as a nucleophile: (A) (В) H H. H (D) H-C-H (C) H -N- H H -m
A: Introduction: Nucleophile means nucleus loving. That means nucleophile are the molecules which are…
Q: Which molecule can loose a hydrogen and become a nucleophile? Select one: a. H3C– ECH b. H;C- -CH3…
A: The terminal alkynes or 1-alkynes are weak acids and loose a hydrogen when treated with strong base…
Q: Br. `NH2
A: Answer -
Q: the reaction below, which face of the carbonyl did the nucleophile (SH) add to? HS O SH
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Q: Identify the stronger nucleophile in the following pair ? CH3NH2, CH3OH
A: The CH3NH2 has a lone of electron over the amine which is unhindered and won’t not donate the…
Q: LOH (RL NaOH (S) H2O This nucleophilic substitution occurs with rearrangement. Draw curved arrows to…
A: In this question, we will write the Nucleophilie reaction mechanism by using carved arrows. You can…
Q: Which of the following statements is INCORRECT? Select one: O a. Ethoxide is a better nucleophile…
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Q: Br CH;OK a) b) Sn1 Sn2 c) d) E1 E2
A: Generally, alkyl halide or alcohols undergo elimination reaction which give rise to alkene.…
Q: Determine the HOMO in the nucleophile and LUMO in the electrophile in the reaction below. NH, Me…
A:
Q: H H N H H CL H H
A: Step 1: The strong nucleophile attacks on the electrophile which is alkyl halide. Step 2: leaving…
Q: In an Sn2 reaction with "CN as nucleophile, [CH:CH:CI | CH:CH;OH_ CH;CH;0Tos] reacts faster because…
A: CH3CH2oTosl react faster beacuse it has better leaving group than the other ones. These type of…
Q: pp. but-1-en-3-one + NaCN 1. React the carbonyl compound: It is (circle one) CONJUGATED…
A: The reaction of but-1-en-3-one with NaCN is as follows:
Q: NaBH4, NICI2 is a O soft electrophile O hard nucleophile hard electrophile O soft nucleophile
A:
Q: Circle which of the following ions will be good leaving groups in sn1 and sn2 reactions?
A: Leaving group is the one that accepts a lone pair when the bond between it and its neighbouring…
Q: Which of the following is not a nucleophile? (Circle one answer). a. Н2О b. CH30- ntherate с. NH3 d.…
A: Nucleophile, is an atom or molecule that in chemical reaction want a positive centre, such as the…
Q: Identify the stronger nucleophile in the following pair ? NH3, −NH2
A: Nucleophilicity is defined as the tendency to give the electrons. Species with negative charge will…
Q: most stable to least stable nucleophiles
A: Nucleophiles are the chemical species which are nucleus loving and donates an electron pair to form…
Q: alkenes possessing five carbons or fewer. OEt ethyl acetoacetate or EtO OEt diethyl malonate and…
A:
Q: a. Rank in order of S2 reactivity (1= most reactive) b. Rank in order of leaving group ability (1=…
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Q: Draw the product of nucleophilic substitution with attached neutral nucleophile. When the initial…
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Q: Place reagent combinations in the out to successfully carry the following transformation. ? Ph Ph…
A: Lithium aluminium hydride is strong reducing agent...it reduces azide into primary amine..... R-N3…
Q: HO HO но SH
A: Nucleophilicity is an ability of the particular nucleophile to attack on the electrophilic center.
Q: O strong nucleophile in an aprotic solvent O strong nucleophile in a protic solvent O weak…
A:
Q: Select the strongest nucleophile from the list below. OH O CF O HS-
A: The species which have tendency to donate electron pair and are electron rich in nature is known as…
Q: Which is the best leaving group for an SN2 reaction? O F- O C- O Br-
A: To identify: The best leaving group for an SN2 reaction.
Q: What is the nucleophile in the following reaction? 2H20 + CH3I → CH;OH + F + H30* O CH3I O CH3OH O…
A: In an organic chemical reaction, there are nucleophiles and electrophiles. These are substances that…
Q: Please answer this question
A: Nucleophiles are the molecules or substances that have tendency to donate electrons or react with…
Q: In the following reaction which species acts as the nucleophile? OCH,CH3 (H3C),N, CH;CH,OH OCH,CH3…
A: Since you asked multiple question we will solve first question for you. If you want to specify…
Q: Which of the following is the strongest nucleophile? OH- H20 H2S HS-
A: Answer :- HS- -------------------------------------
Q: Rank these nucleophiles from best to worst Na- I -I Best (II)>(1)>(III) worst Best (1)>(III)>(II)…
A: A question based on introduction to organic chemistry that is to be accomplished.
Q: Rank the nucleophiles from weakest to strongest. (1 = weakest, 3 = strongest) HOH
A: Nucleophiles are capable of donating electron pair for forming a bond. The measure of strength of…
Q: Type of nucleophile suitable for SN2 & SN1 reactions & 3 examples SN2 SN1
A: SN2 & SN1 are two types of nucleophilic substitution reaction, in which a nucleophile attacks…
Q: Which of the two is the stronger nucleophile? Select one: a CH3OH b. CH3O Which is a polar aprotic…
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Q: Circle the reactant that is a nucleophile and draw the mechanism using the appropriate arrows for…
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Q: Can you match best nucleophile / conditions that will give a successful hydrolysis reaction for each…
A: For the given electrophile, acid chloride and acetic anhydride, water is used for the hydrolysis…
Q: SN1 SN2 Br YES (example) (ехample) SECONDARY (SUBSTRATE) YES YES TOSYLATE (OTs) GOOD (LEAVING GROUP)…
A: ITs entirely depends upon the Reaction conditions whether an Sn1 or Sn2 Reaction will occ.
Q: .2 Circle the best choice for each statement. La to Best Substrate for SN1 Best nucleophile in DMSO…
A: There are some molecules . We have to tell and give explanation the best solvent for SN1 and SN2…
Q: In which category does NaNHCH2CH3 belong? А. Good nucleophile, weak base. В. Good nucleophile,…
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Q: ® Identify which is nucleophile / electrophile. Identify if it is neutral or charged nucleophile or…
A: Nucleophile - A nucleophile is the compound which consists of electrons as lone pair available for…
Q: NABH4 CH3OH + H,O NH2 Draw the product of each step. NH2 draw structure .. proton transfer
A: Applying concept of reduction followed by proton transfer and cyclisation reaction.
Q: HCOO- > HO- > (CH3)2 Sort from best nucleophile to worst nucleophile
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Q: Label the electrophilic and nucleophilic sites in attached each molecule ?
A: A chemical reaction is symbolic representation of the conversion of substances to new substances. In…
Q: Which of the following is the strongest nucleophile? CH3S OH- H20 CH3O¯ NH3
A: Nucleophiles A Nucleophile is a chemical species that donates an electron pair to form a…
Q: Consider the reaction below. [1] Draw curved arrows to show the movement of electrons in each step.…
A: #13: The reactant is a protonated alcohol and the product is an alkyl chloride. The reaction shows…
Q: Are the following nucleophiles, electrophiles, they be both a nucleophile or electrophile, or…
A: Nucleophiles are those species which are electron rich and hence can donate electron pairs to the…
Q: Which factor below does NOT influence the rate of an SN2 reaction. O nature of the solvent O steric…
A:
Q: (c) With increasing nucleophilicity (1: least nucleophilic; 3: most nucleophilic) ОН CHO.
A: Given nucleophilicity order
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- A student proposes the following reaction mechanism for the reaction in Model 6. Which step inthis mechanism is least favorable? Explain your reasoning.Plastic photochromic sunglasses are based on the following reversible rearrangement of a dye inside the lenses that occurs when the lenses are exposed to sunlight. The original dye absorbs UV light but not visible light and is thus colorless, while the rearrangement product absorbs visible light and is thus darkened. (a) Show the mechanism of the rearrangement. (b) Why does the rearrangement product absorb at a longer wavelength (visible light) than the original dye (UV)?The reactants, intermediates, final products, and all curved arrows showing bonds forming andbreaking are collectively referred to as the mechanism of a reaction. For the following reactants: a. Explain why the original statement of Markovnikov’s rule does not help in this case, but themodern restatement of Markovnikov’s rule tells you which carbon will get the X (Cl). b. Show the mechanism of the most likely addition reaction between the reactants.