why was the tertary butyl

  1. why was the tertary butyl chloride washed with aqueous sodium hydrogen carbonate? what gas was evolved during the washing? write
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    2. conway asked by conway
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  2. How can I rank these substrates from fastest to slowest reacting? In an SN2 reaction with NaI-Acetone? Based on theory alone?ben
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    2. helllp asked by helllp
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  3. Just want to make sure that my thought process is right on this one.5 compounds: n-butyl chloride n-butyl bromide sec-butyl
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    2. ramire2 asked by ramire2
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  4. We did an experiment with the synthesis of n-butyl bromide, using n-butyl alcohol, NaBr, and H2SO4. The question is: Aqueous
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    2. CMM asked by CMM
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  5. Describe how you would prepare t-butyl-n-butyl ether. assume you are working on a 1 M scale. what reagents would you use? What
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    2. HELP asked by HELP
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  6. Used the information below to solve for the therotical yield of n-butyl AcetateTheoretical yield of n-butyl acetate = (Molecular
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  7. 1if you open the tert-butyl chloride and tert-butyl bromide to the air for few hours? What happened to the ratio of the halide
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    2. jenny asked by jenny
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  8. When synthesizing n-butyl bromide by allowing n-butyl alcohol to rect with sodium bromide and sulfuric acid what are the
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    2. Tammy asked by Tammy
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  9. when di-n butyl ether and hot concentrated naoh react----> nor rxn .. why?when di n butyl ether reacts with na metal---> nor
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    2. lou asked by lou
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  10. 1. Can I2 react with Cyclohexane to form any product (without or without spectroscophic properties)?2. Can I2 react with t-butyl
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    2. John asked by John
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