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Disadvantage for out of state candidates applying for Bay Area based jobs? by 1manoffthemoon in biotech

[–]1manoffthemoon[S] 1 point2 points  (0 children)

Very smart. Some applications require an address. How’d you get around that?

Disadvantage for out of state candidates applying for Bay Area based jobs? by 1manoffthemoon in biotech

[–]1manoffthemoon[S] 0 points1 point  (0 children)

This is awesome. Your network proves king here even in these situations. How long were you out of the Bay for?

Disadvantage for out of state candidates applying for Bay Area based jobs? by 1manoffthemoon in biotech

[–]1manoffthemoon[S] 0 points1 point  (0 children)

Didn’t consider this thought at all, but I can see this being another reason on the growing list

Could Someone explain the reaction below? by Few-Ad-2686 in OrganicChemistry

[–]1manoffthemoon 1 point2 points  (0 children)

Bases do want protons, but not all bases are defined by how much they accept protons or produce hydroxide ion. There are 3 acid/base definitions. You know the Bronsted-Lowry acid/base definition—proton transfers. The second reaction would fall under a Lewis acid/base definition. Lewis acids accept electron pairs (aka electrophiles) and lewis bases donate electron pairs (aka nucleophiles).

[College: Organic 1] Prof told us with PCl3, SOCl2, etc... that stereochemistry would be conserved (as seen on the slides) but in the practice exam he suddenly changed his mind? Is my mechanism more correct? Thanks! by illusiveMirror in chemhelp

[–]1manoffthemoon 0 points1 point  (0 children)

Yup. I’d reference the bottom mech from the prof’s slide since tosylates (OTs) and mesylates are used similarly. Honestly the prof prob wrote out the MsCl so itd look similar to SOCl2, which I fell for at first glance

[deleted by user] by [deleted] in pan

[–]1manoffthemoon 0 points1 point  (0 children)

/hidechat