--%>
Assignment Help - homework help

base

parachloroaniline is strong base than paranitroaniline

   Related Questions in Chemistry

  • Q : Group Cations Explain how dissolving

    Explain how dissolving the Group IV carbonate precipitate with 6M CH3COOH, followed by the addition of extra acetic acid, establishes a buffer with a pH of approximately

    		•
  • Q : Amines arrange in order of

    arrange in order of basicity,pyridine,pipyridineand pyorine

    		•
  • Q : Normality of sulphuric acid Help me to

    Help me to go through this problem. Normality of sulphuric acid is: (a) 2N (b) 4N (c) N/2 (d) N/4

    		•
  • Q : Difference among hcl gas and hcl acid

    What is the basic difference among hcl gas and hcl acid? Briefly state the difference?

    		•
  • Q : What is cannizaro reaction? Explain

    Aldehydes which do not have  -hydrogen atom, such as formaldehyte and benzaldehyte, when heated with concentrated (50%)alkali solutio

    		•
  • Q : Explain the mechanism of Enzyme

    A mechanism for enzyme-catalyzed reactions that leads to the typical rate equation for these reactions can be described.A variety of rate equations are required to portray the rates of enzymes catalyzed reagents and physical conditions that are encountered

    		•
  • Q : Structure of a DNA molecule Elaborate

    Elaborate the structure of a DNA molecule?

    		•
  • Q : Tetrahedral holes In zinc blende

    In zinc blende structure, zinc atom fill up:(a) All octahedral holes  (b) All tetrahedral holes  (c) Half number of octahedral holes  (d) Half number of tetrahedral holesAnswer: (d) In zinc blende (ZnS

    		•
  • Q : What is Flash Photolysis Reactions.

    An example illustrates the type of mechanism that can be written to explain the development of flash photolysis reactions. Often, as the reactions in the ozone layer of the earth's atmosphere, we are interested in the kinetic behavior of species that are not a

    		•
  • Q : Explain the preparation of phenols. The

    The methods used for the preparation of phenols are given below:    From aryl sulphonic acids

    		•