The NH group is more reactive than the OH group because the lone pair on nitrogen in NH group is less stable due to the higher electronegativity of nitrogen compared to oxygen. This makes the lone pair in the NH group more readily available for reactions compared to the OH group. Additionally, the smaller size of nitrogen allows for stronger interactions with other atoms or molecules, increasing reactivity.
Amide bonds involve a carbonyl group (C=O) and an amino group (NH2) functional group.
The main functional groups in oxymetazoline are an ether group (-O-) and an amine group (-NH-). The amine group can be part of an amide or imine functional group.
Though it is hardly soluble in water, I would chemically consider OC (pepperspray, (CH3)2CHCH=CH(CH2)4CONHCH2C6H3-4-(OH)-3-(OCH3) as weak base rather than acid, the amide CONH-group being the most significant group which is more base (C-NH) then acid (C=O).
Diphenylamine has a simple structure consisting of two benzene rings connected by an amino group (-NH-). Each benzene ring has a phenyl group attached to it.
Yes
The OH bond is more polar than the NH bond because oxygen is more electronegative than nitrogen, leading to a greater difference in electronegativity between oxygen and hydrogen. This means the OH bond has a greater separation of charge and greater polarity than the NH bond.
nh-ch3
The amino group in p-aminophenol would react first with acetic anhydride because it is more nucleophilic compared to the hydroxyl group. The lone pair of electrons on the amino group can attack the electrophilic acetic anhydride, forming an amide linkage.
The functional groups in phacetin are an ester group (-COO-), an amide group (-NH-), and an aromatic ring.
The systematic name of NH₄ClO₃ is ammonium chlorate. In this compound, NH₄⁺ represents the ammonium ion, while ClO₃⁻ is the chlorate ion. The name reflects the combination of these two ions, indicating the presence of ammonium and the chlorate functional group.
Well, usually it will take three days to get from NH to NC. But there is no definite time frame that a letter to reach a destination. It all depends and usually considered that it will not ake more than a week.
Amide bonds involve a carbonyl group (C=O) and an amino group (NH2) functional group.
The functional groups in paracetamol include an amide group (-NH-CO-), a phenol group (-OH), and an aromatic ring system.
The main functional groups in oxymetazoline are an ether group (-O-) and an amine group (-NH-). The amine group can be part of an amide or imine functional group.
don't know if they are in NH yet, but here is some more information about them... http://www.elubin.com/webkins/charms.asp
Though it is hardly soluble in water, I would chemically consider OC (pepperspray, (CH3)2CHCH=CH(CH2)4CONHCH2C6H3-4-(OH)-3-(OCH3) as weak base rather than acid, the amide CONH-group being the most significant group which is more base (C-NH) then acid (C=O).
Diphenylamine has a simple structure consisting of two benzene rings connected by an amino group (-NH-). Each benzene ring has a phenyl group attached to it.