Draw the starting alkyne that would lead to the following two products under these conditions. Select to Draw 1. KMnO4, OH¯ (warm) 2. H3O+ HO OH
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- What is the product (A, B, C, or D) of the reaction shown in Image30? a. C b.D c. B d. APlease draw the possible resonance structures for the following carbocations. Please demonstrate the relative stability of each carbocation. (Ex. An allylic secondary carbocation is more stable than a primary carbotion.)1. When you add H-Br in a terninal alkene, the product has the rule od Markovnikov? 2. The type pf intermetary thag forms when we add HgSO4/H2SO4/H2O in an alkyl is? Please solve my both questions.thank you.
- Which is most basic leaving group among the listed below? a. –O–CO–R b. –NH2 c. –O–R d. Cl–What the major product of the following reaction? (Don't use hand raiting please)When an unsymmetrical Alkenes such as propane is treated with N-bromosuccinimide in aqueous dimethyl sulfoxide, the major product has the bromine atom bonded to the less highly substituted carbon atom. Is this Markovnikov or non-Markovnikov orientation? Show its complete reaction mechanism.
- What are products formed from the below reaction? Draw the stereoisomers and name them. (There are two different constitutional isomers and each constitutional isomer has 2^n stereoisomers.) Please solve the problem in detail.Draw the three likely products of the following reaction. Identify the major product.Arrange the following three compounds below with regard to their ease of undergoing an SN1 reaction. Draw the relevant structure(s) to justify. Place the fastest one on top