(a)
Interpretation:
The product obtained in the reaction of 3-acetylfuran with nitric acid and sulfuric acid has to be given.
Concept Introduction:
The reaction of sulfuric acid and nitric acid results in the generation of nitronium ion which attacks the most nucleophilic position of the reactant. The nucleophilicity of the carbon atoms present in the furan depends upon the nature of substituents attached to it.
(b)
Interpretation: The product formed in the reaction of 2-nitrothiophene with bromine has to be given.
Concept Introduction:
The reaction of bromine with alkyl and aryl groups is a type of electrophilic substitution reaction in which
(c)
Interpretation: The product obtained in the reaction of 4-dimethylaminepyridine with methyl iodide has to be given.
Concept Introduction:
Tertiary
(d)
Interpretation: The product obtained in the reaction of pyridione with
Concept Introduction:
Phosphorus trichloride reacts with hydroxyl group and leads to the formation of
(e)
Interpretation: The product obtained in the reaction of 1,4-dimethylpyridine hydroxide with formic acid and hydrochloric acid has to be given.
Concept Introduction:
Tertiary amines exist as quaternary ammonium salts in the electrolytic solution. Quaternary ammonium salts are the salts of nitrogen in which four groups are attached to nitrogen and it exhibits a positive charge which is stabilized by the negative charges present in the solution.
(f)
Interpretation: The product obtained in the reaction of pyrrole with
Concept Introduction:
The alkyl group attached to magnesium bromide acts as a nucleophile because carbon atom is more electronegative as compared to magnesium due to which carbon atom exhibits partial negative charge in the reaction of Grignard reagent.
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Organic Chemistry, Books a la Carte Edition (8th Edition)
- The velocity distribution function of gas moleculesa) is used to measure their velocity, since the small size of gas molecules means that it cannot be measured in any other wayb) is only used to describe the velocity of particles if their density is very high.c) describes the probability that a gas particle has a velocity in a given interval of velocitiesarrow_forwardExplain why in the representation of a one-dimensional velocity distribution function for a particular gas, the maximum occurs for vi = 0 m/s.arrow_forwardExplain why the representation of a one-dimensional velocity distribution function for a particular gas becomes flatter as the temperature increases.arrow_forward
- Draw a Lewis structure for each of the following molecules and assign charges where appropriate. The order in which the atoms are connected is given in parentheses. a. CIFCIF b. BrCNBrCN 0 c. SOCI2 × (CISCIO) SOC₁₂ (CISCI) You can draw both an octet and a valence shell expanded structure. Considering the following structural information, which is the better one: The measured S-OS-O bond length in SOC12SOCl2 is 1.43 Å. For comparison, that in SO2SO2 is 1.43 Å [Exercise 1-9, part (b)], that in CHзSOHCH3 SOH d. CH3NH2CH3NH2 (methanesulfenic acid) is 1.66 A. e. CH3OCH3 CH3 OCH3 NH2 f. N2H2× (HNNH) N2 H2 (HNNH) g. CH2COCH₂ CO h. HN3× (HNNN) HN3 (HNNN) i. N20 × (NNO) N2O (NNO)arrow_forwardbre The reaction sequence shown in Scheme 5 demonstrates the synthesis of a substituted benzene derivative Q. wolsd works 2 NH2 NaNO2, HCI (apexe) 13× (1 HNO3, H2SO4 C6H5CIN2 0°C HOTE CHINO₂ N O *O₂H ( PO Q Я Scheme 5 2 bag abouoqmics to sounde odi WEIC (i) Draw the structure of intermediate O. [2 marks] to noitsmot od: tot meinedogm, noit so oft listsb ni zaupaib bas wa (ii) Draw the mechanism for the transformation of aniline N to intermediate O. Spoilage (b) [6 marks] (iii) Identify the reagent X used to convert compound O to the iodinated compound [tom E P. vueimado oilovonsa ni moitos nolisbnolov ayd toes ai tedw nisiqx (iv) Identify the possible structures of compound Q. [2 marks] [2 marks] [shom 2] (v) bus noires goiribbeolovo xnivollot adj to subora sidab Draw the mechanism for the transformation of intermediate P to compound Q. [5 marks] vi (vi) Account for the regiochemical outcome observed in the reaction forming compound Q. [3 marks]arrow_forwardPROBLEM 4 Solved Show how 1-butanol can be converted into the following compounds: a. PROBLEM 5+ b. d. -C= Narrow_forward
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