O Example 6. Use a Grignard's reagent to prepare the following alcohols: (a) 2-Phenyl butan-2-ol (c) 2-Methyl pentan-2-ol (e) 3-Methyl-1-phenyl butan-1-ol. (b) 3-Methyl pentan-3-ol (d) 2-Phenyl propan-2-ol

Q: Provide the structure of the major product(s) of the followings organic reactions: a) b) c) -CEC…

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Q: 10. Devise a synthesis of each product from the given starting material. More than one step is…

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Q: Draw the reaction and its products

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Q: 1. Name the following alcohols using IUPAC Rules. ОН (b) Br-CHCH, ОН (с) ОН ту

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Q: Draw and name all constitutionally isomeric alcohols with the molecular formula C4H10O

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Q: With 2° or 3° alkyl groups bonded to the ether oxygen, the C—O bondis cleaved by an SN1 mechanism…

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Q: Use a Grignard reaction to prepare the following alcohols: (a) 2-Methyl-2-propanol (b)…

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Q: b) Complete the scheme for the synthesis of an important ether.

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Q: 1) Provide a 3-step synthesis to get the following product. o-ly by H 2) Which of the following…

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Q: a.) H- C = C-H CH3 - C=C- CH2-CHz -CH2-CH3 b.) CH3 - C Hz- CH2- OH H3c-C三c-H C.) CH= CH A CH3 -…

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Q: Which carbonyl groups in the following reactions would require protection? (a) (b) 1. NaNH, Mg(s) Br…

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Q: Which of the following is a ketone? O A. (CH3)2CHOH В. Снзсоснз3 С. Снзсно D. CH3CH20CH3

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Q: Choose the BEST reagent for carrying out the following conversion. A NaOH, H₂O (B) NaBH4 CH₂PPh3 All…

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Q: Name the following ethers by IUPAC rules:

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Q: 7) Name at least 3 sets of reagents that can carry out the following conversion. Include the sodium…

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Q: (а) -C- -ОН (b) -0-CH3 (c) -CI (d) C-CH3 (е) -NH3

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Q: B2. (i) Draw a complete arrow pushing mechanism for the following reaction. You can assume that the…

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Q: (b) 1,2-hexanediol Draw the structure of the alkene that was used to prepare the alcohol in highest…

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Q: What is the major product that results from the following reaction? Br -ONa ? (A) (B) (C) (D) O A ов…

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Q: 8) Show how the following conversions might be accomplished, including all reagents and…

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Q: 12.60 Predict the major product of the following reaction. no ? CN O NaCN acetone

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