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Did u try googling it??y r tertiary alcohols resistent to oxidation?
how is the substitution reaction of an alcohol wit a hydrogen halide a nucleophilic substitution?cuz as far as i noe -nucleophiles are electron donors so wer is the donation of electrons taking place here??
thnxxxx....dat helped..Did u try googling it??
nywy...The answer to this question depends on your point of view. From a thermodynamic point of view tertiary alcohols are resistant to oxidation, due to the fact that C-C single bonds are stable. Simply speaking, a carbon atom surrounded by three further carbon atoms and a C-O single bond will be more stable than a carbon atom surrounded by two carbon atoms and a C=O group. Quantum mechanical (ab-initio) calculations show that C-C single bonds are slightly electron donating with respect to each other, this means that the central carbon atom of a tertiary alcohol will be more stable than its oxidised analogue - therefore tertiary alcohols are resistant to oxidation under standard conditions.
One thing to note! Tertiary alcohols are only resistant to oxidation under standard conditions with mild oxidising agents - oxidation of tertiary alochols is possible, albeit under quite extreme conditions.
its a nucleophilic substitution bcoz d C atom bonded to the hydroxyl grp will carry a partially positive charge (diff in electronegativity of O n C).how is the substitution reaction of an alcohol wit a hydrogen halide a nucleophilic substitution?cuz as far as i noe -nucleophiles are electron donors so wer is the donation of electrons taking place here??
yaaa that helped..!! A LOOT!!its a nucleophilic substitution bcoz d C atom bonded to the hydroxyl grp will carry a partially positive charge (diff in electronegativity of O n C).
This makes it open to nucleophilic attack. ie the partially -ve halogen atom in hydrogen halide will attack the bond btw the C n hydroxyl grp..
Hope i helped!!
For Question 11 you can see that the equilibrium concentration of Z decreases as the temperature is increased. This means that increasing the temperature lowers the forward reaction (or more simply the Kc for the reaction), and you must remember that Kc for exothermic reaction decreases with increasing temperature (because exothermic gives out heat energy)Anyone explain these two questions to me please? Thanks first! :Yahoo!:
FYI, the answer given for Q10 is D whereas for Q11 is D.
yaaa that helped..!! A LOOT!!
(i kinda tend to miss the most obvious stuff..!!)
thnx once again
Ammonium nitrate, NH4NO3, can decompose explosively when heated.
NH4NO3 → N2O + 2H2O
What are the changes in the oxidation numbers of the two nitrogen atoms in NH4NO3 when this
reaction proceeds?
A –2, –4 B +2, +6 C +4, –6 D +4, –4
For 8, find the mass of Cl2 ie 5.287 - 2.920 = 2.367gQ-6, 8, 9, 10, 18, 25, 35
http://www.xtremepapers.com/papers/... AS Level/Chemistry (9701)/9701_s10_qp_11.pdf
http://www.xtremepapers.com/papers/... AS Level/Chemistry (9701)/9701_s10_ms_11.pdf
i believe its the 3rd time i'm posting :/
Can anyone explain this question?Q21 How does the compound have 5 double bonds. I counted 6(one in the side chain and 5 in the cyclohexene ring due to presense of just one hydrogen in it.)
Ammonium nitrate, NH4NO3, can decompose explosively when heated.
NH4NO3 → N2O + 2H2O
What are the changes in the oxidation numbers of the two nitrogen atoms in NH4NO3 when this
reaction proceeds?
A –2, –4 B +2, +6 C +4, –6 D +4, –4
the greater the ph value the weaker the acid..rit?For 10, look at the pH values given for X n Y...
This shows that X is an acid - pH =pH below 7, n Y is a base pH abv 7.
Student P says that X is a strong acid which is completely wrong, as strong acids do not have such a high pH..
However Q says tht Y dissociates more, n since Y is a base, we shud know tht the greater the value of pH, the stronger the acid..
Y is 2 nos greater thn 7, n X is only 1 no lesser thn 7...this shows tht Y is a stronger base n dissociates more..
Hence Q only is correct..
Ya noww i get it. well you know you asked this one at school and you drew the whole thing. only problem was i didnt think there would be any other double bond in the chain but only in the cyclohexene ring. But it was supposed to be the opposite. well thanks.Did it for you (sorry, diagram doesn't really look good) -
Then
Defend nhin kr rhi..han han.. kar lo defend apnay aap ko...
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