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Explain why the following cyclohexanol A derivative undergoes E2 more readily than cyclohexanol B. State three reasons.
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- 1. Br + CH3O°Na* methanol 2. CI NH3 ethanol 3. CI CH3 O'Na* ethanolDraw a conclusion as to its water solubility. use carbon ration rule and functional groups HO OH N. CH35. Complete each of the following reactions by providing the line/angle structure of the major organic product where there is a question mark. кон ? H20 Salt Carboxylic acid Base H но b) OH Alcohol Ester Carboxylic acid
- Draw the product of the reaction between a ketone and an alcohol. Include all hydrogen atoms in the product. རྐང་པའི H* +1 mole equiv. CH, HỌ CH, CH Select Draw Rings More G c Q2Q Erase How would you classify the product of the reaction? Note that a hemiacetal formed from a ketone is also called a hemiketal; an acetal formed from a ketone is also called a ketal. 00 The product is a ketone. The product is a hemiketal. The product is an alcohol. The product is a ketal.Which of the following is a secondary alcohol? O A. но CH3 CH2CH3 В. CH2CH2CH3 CH3 CH2-C-CH2CH3 Он O C. CH3 CH 2-CH-CH3 Он D. CH3CH2-CH-CH2CH2CH3 ČH2CH2CH2OHHow could we separate a mixture of benzoic acid and cyclohexanol?
- The name of this organic compound. CH,CH,-C-CH,-CHO O 3-ketopentanal 3-oxobutanal 3-oxopentanal O 3-pentanone The type of this organic compound. Ochiral ketone symmetrical ketone achiral ketone unsymmetrical ketone10 Regarding t-butanol and n-butanol, which is/ are correct statements of the following: |- Both are having equal solubility in water Il- t-butanol is more soluble in water than n- butanol III- Boiling point of t-butanol is lower than n-butanol IV- Boiling point of n-butanol is lower than t-butanol * Only I Only II Only II Il & II III & IVhow to convert 1-butanol into 4-heptanol