During the reaction of glucose and fructose with excess phenylhydrazine to form osazone, only the C-1andC-2 atoms of glucose and fructose participate in the reaction. The rest of the molecule remains intact. Hence, glucose and fructose produce the same osazone.
Answer:
92.6
Explanation:
6 mol x 18.02 g of H2o --> 3 mol x 58.33 g Mg(OH)2
108.12 g of h2o --> 174.99 of Mg(OH)2
g of H2O is 150 g of Mg(OH)2
150g x 108.12g / 174.99 =
92.67
Answer:
C) SN2 and E2
Explanation:
For this question, we have analyzed the <u>substrate</u> and the <u>base/nucleophile</u>. The substrate, in this case, is 1-iodohexane and the base/nucleophile is potassium tert-butoxide.
<u>Substrate</u>
<u />
In the 1-iodohexane the iodide "I" is bonded to a primary carbon (carbon 1). Therefore we will have a <u>primary substrate</u>. If we have a primary substrate an Sn1 can not take place. We can not have a <u>primary carbocation</u> due to this instability. So, we can disccard options A) and B).
<u>Base/nucleophile</u>
<u />
In the potassium tert-butoxide we have an ionic compound. A positive charge is placed in the potassium atom a negative charge is placed in the oxygen of the ter-butoxide ion. So, we will have a <u>strong base</u> (a molecule with the ability to remove electrons) and a <u>strong nucleophile</u> (a molecule with ability to bond with an electrophile). With all this in mind, w<u>e can not have an E1 reaction</u>.
With both analyses, the answer is C).
See figure 1
I hope it helps!