iTeachChem
A Study Community for Everyone and Everything. We have weekly sessions on Spirituality, Math and Science! JEE, NEET prep? All doubts are crowdsourced. Hare Krishna!
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iTeachChem
A Study Community for Everyone and Everything. We have weekly sessions on Spirituality, Math and Science! JEE, NEET prep? All doubts are crowdsourced. Hare Krishna!
Join
basic amine doubt
hello arent the left nitrogen lone pairs conjugated and the same with the right side upper nitrogen so i expected one of the pyridine type nitrogens to donate but its not,
amines 4
har ek step btado kya hoga, socl2 vala pata mereko,k2cr2o7 oxidising agent ha ye bhi pata ha bs
Stability of Carbanions
Do we consider the hyperconjugation exerted by the methyl group (even though Hyperconjugation results in an increased stability of Carbocations. Alkenes and Radicals only) ? If so, the order of stability would be: 2 > 3 > 1. If not, the order of stability would be: 3 > 2 > 1
substitution on diazochloride
uhh idk if my thought process is ok on this one, the ring is attaching to the right side of beneze due to lower steric repulsion? and not the top?
rc circuit- capacitors
i dont think any of the options is right. the latter pic is what i feel the graph should be like. Is it right? like shouldnt it dip while discharging unlike opt 1 which is the correct ans. it wont drop to 0 so 3 is incorrect too
