b) The diagram below shows the reaction scheme for benzene and its derivatives: соон CH,CI, AICI, Br2, uv Y i) Draw compound X. ii) What reagents are required to carry out the conversion I and II ? iii) Name compound Y
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- Below are two potential methods for preparing the same ether (Option A and B), but only one of them is actually successful. Identify the successful approach (A or B)a) Write out the 3-step arrow pushing mechanism showing how 1-pentene is hydrated to make 2-pentanol. b) Draw the other 2 alkenes(don’t forget cis/trans isomers!) that could also be hydrated to make 2-pentanol. Briefly explain why1-pentene is the best choice.Below is a schematic representation of possible reactions that Compound X can undergo. Use the scheme to answer the following questionsA)What is the IUPAC name for Compound X?B)What type of reaction (s) is/are represented by (i) and (ii)?C)Compound X undergo transitions through either [A] or [B] to produce compounds [1], [2], [3] and [4]. Draw the structures of [A] and [B]. D)Illustrating with reaction mechanisms, show how compounds [1], [2], [3] and [4] are formed.E)Which of the compounds in the following pairs will occur in relatively higher yields and why?I)[1] and [2] II)[3] and [4]
- 1. Include reagents 2. Include mechanisms usedBelow is a schematic representation of possible reactions that Compound X can undergo. Use the scheme to answer the following questions. A. What is the IUPAC name for Compound X? B. What type of reaction (s) is/are represented by (i) and (ii)? C. Compound X undergo transitions through either [A] or [B] to produce compounds [1], [2], [3] and [4]. Draw the structures of [A] and [B]. D. Illustrating with reaction mechanisms, show how compounds [1], [2], [3] and [4] are formed. E. Which of the compounds in the following pairs will occur in relatively higher yields and why? [1] and [2] [3] and [4] The attached image contains the scheme.Below is a schematic representation of possible reactions that Compound X can undergo. Use the scheme to answer the following questions. –a. What is the IUPAC name for Compound X? b. What type of reaction (s) is/are represented by (i) and (ii)? c. Compound X undergo transitions through either [A] or [B] to produce compounds [1], [2], [3] and [4]. Draw the structures of [A] and [B]. d. Illustrating with reaction mechanisms, show how compounds [1], [2], [3] and [4] are formed.e. Which of the compounds in the following pairs will occur in relatively higher yields and why?i. [1] and [2] ii. [3] and [4]
- Using any necessary organic and inorganic reagents, show how you can carry out the chemical conversions shown below. Please answer parts a, and b.1. Which compound is expected to have a higher melting point, 1-pentanol or 1-pentanal? Explain 2. Which compound is expected to be more soluble in water, propanal or butanal? Explain. 3. Why is acetyl chloride more reactive towards hydrolysis than ethyl acetate?Show how to prepare each alkyne from the given starting material. In part (c), D indicates deuterium. Deuterium-containing reagents such as BD3, D2O, and CH3COOD are available commercially.
- Below is a schematic representation of possible reaction that compound X can undergo.Use the scheme to answer the following questions. A.What is the IUPAC name for compound X B. What type of reactions is/are represented by (i) and(ii). C.Compound X undergo transitions through either (A) or (B) to produce compounds (1),(2),(3) and (4). Draw the structure of (A) and (B).Illustrated below is the hydrolysis of a C-C bond (in the first molecule) hydrolyzed by water (2nd molecule). Which pair of open boxes best identifies the location of the (-H) and (-OH) components of water on the products. Choose one from the following: (a) A (b) B (c) C (d) DWhat is reaction 1 and 2 called? Choices: A. Williamson ether synthesis, B. Reduction with Grignard reagent, C. Acidic ether cleavage, D. FC Alkylation What are the reagents for reaction 1 and 2? Choices: A. methanol in acidic medium, B. sodium hydride and bromomethane, C. methyl bromide and aluminum bromide, D. methanoyl bromide