Compounds x and y are both c5h11cl products formed in the radical chlorination of pentane. base-promoted e2 elimination of x and y gives, in each case, a single c5h10 alkene (ignoring double bond stereochemistry). both x and y react in sn2 fashion with sodium iodide in acetone; y reacts faster than x. what is the structure of y? g

The organism shown is a free-living one that is anchored to the bottom of ponds and streams during one stage of its life cycle what is the common name for the group to which this organism belong

The boiling point of propanoic acid is higher than that of 1-butanol because: propanoic acid has a higher molecular weight than 1-butanol. propanoic acid is more soluble in water than 1-butanol. propanoic acid is a better hydrogen bond donor than 1-butanol. propanoic acid forms hydrogen bonded dimers and 1-butanol does not. 1-butanol forms hydrogen bonded dimers and propanoic acid does not.

Which of these conditions most likely produces an unstable isotope?