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-1 units The sparse solubility of MNTS in water results in a negligible rate of acid hydrolysis in the aqueous pseudo-phase. This was previously observed in the nitroso group transfer from MNTS to amines in ternary (ref. 47) and quaternary microemulsions (ref. 31)
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The small inhibitory effect observed in the nitrosation of piperazine may have resulted partly from the statistical advantage of possessing two equivalent nitrosable positions in an environment of limited mobility such as the microemulsion interface. The effect on the nitrosation of MeBzAm (viz. a decrease of approximately 60 times in the rate constant relative to water) was similar to that previously observed in the nitrosation of amines by alkyl nitrites (see ref. 46)
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