(a). Why is `beta-D-`gllucopyranose the most abundant of naturally occurring aldohexoses?
(b). Write the most stable chair conformer for `alpha-D-` fructopyranose. How does it dirrer from `beta-`anomer?
(a). Why is `beta-D-`gllucopyranose the most abundant of naturally occurring aldohexoses?
(b). Write the most stable chair conformer for `alpha-D-` fructopyranose. How does it dirrer from `beta-`anomer?
(b). Write the most stable chair conformer for `alpha-D-` fructopyranose. How does it dirrer from `beta-`anomer?
Text Solution
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All the ring substituents in the chair conformation are equatorial.


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