H3C NH2 O represents the chemical formula for dimethylamine oxide, an organic compound commonly used as a protecting agent in the chemical industry. It acts as a stabilizer for certain types of reactive chemicals and helps prevent unwanted side reactions during chemical processes.
One Nitrogen atom = one -NH2. H3C-CH2-CH2-NH2. 1-amino-propane.
Yes they have if they are esters of Carboxylic acids. Eg: Methyl acetate has carbonyl in its middle : H3C-(C=O)-O-CH3
The abbreviation for Acetate is CH3COOH. This is an organic acid.
Reaction: CH3C(=O)CH3 + NH2NHC(=O)NH2 --> (CH3)2C=NNHC(=O)NH2 1) N from NH2 acts as the nucleophile, attacks the carbonyl group and changes into a tetrahedral intermediate. Positive charge on NH2, negative charge on oxygen. (CH3)2(O-C)--(NH2)+NHC(=O)NH2 2) oxygen takes the hydrogen from nitrogen through rearrangement because it is more electronegative. (CH3)2(HOC)--(NH)NHC(=O)NH2 3) Acid protonates the alcohol once more to make it a better leaving group. (CH3)2(H2O+C)--(NH)NHC(=O)NH2 4) Nitrogen from NH2 donates its electrons to generate a double bond, bumping off the water molecule and leaving a positive charge on nitrogen. (CH3)2C=NH+NHC(=O)NH2 5) Water pulls off the hydrogen that was still attached to the nitrogen, thus generating the condensation product between acetone and semicarbazide. (CH3)2C=NNHC(=O)NH2
The compound with the formula H3C-O-CH3 is dimethyl ether, which is an ether consisting of two methyl groups (CH3) connected by an oxygen atom. It can be represented as CH3OCH3. Dimethyl ether is a colorless gas at room temperature and is used as a solvent, a fuel, and in the production of various chemicals.
Ethanoic acid can be converted into methenamine by reacting it with formaldehyde in the presence of aqueous ammonia. This reaction undergoes a condensation reaction to form methenamine as the final product.
ethanol
2-butylhexanoic acid
H3C is a part of the larger compound H3C-CH2-O-CH3, which is ethyl methyl ether, also known as methoxyethane.
One Nitrogen atom = one -NH2. H3C-CH2-CH2-NH2. 1-amino-propane.
2-propylpentanoic acid
esters
H3C is a part of the larger compound H3C-CH2-O-CH3, which is ethyl methyl ether, also known as methoxyethane.
H3c o ch3 ch3
Yes they have if they are esters of Carboxylic acids. Eg: Methyl acetate has carbonyl in its middle : H3C-(C=O)-O-CH3
The abbreviation for Acetate is CH3COOH. This is an organic acid.
Reaction: CH3C(=O)CH3 + NH2NHC(=O)NH2 --> (CH3)2C=NNHC(=O)NH2 1) N from NH2 acts as the nucleophile, attacks the carbonyl group and changes into a tetrahedral intermediate. Positive charge on NH2, negative charge on oxygen. (CH3)2(O-C)--(NH2)+NHC(=O)NH2 2) oxygen takes the hydrogen from nitrogen through rearrangement because it is more electronegative. (CH3)2(HOC)--(NH)NHC(=O)NH2 3) Acid protonates the alcohol once more to make it a better leaving group. (CH3)2(H2O+C)--(NH)NHC(=O)NH2 4) Nitrogen from NH2 donates its electrons to generate a double bond, bumping off the water molecule and leaving a positive charge on nitrogen. (CH3)2C=NH+NHC(=O)NH2 5) Water pulls off the hydrogen that was still attached to the nitrogen, thus generating the condensation product between acetone and semicarbazide. (CH3)2C=NNHC(=O)NH2