The global consumption of synthetic dyes is increasing due to increase in demand in various processing/manufacturing industries.  Analyze why among the large number of organic molecules, only relatively few molecules are considered as dyes. Select any one dye which is used in industry and give justification of type of the dye, its application in the industry and related reactions.

* 52% 20:08 336551-el... Not saved yet a) Work in pairs. Discuss which of these species could qualify as electrophiles and why. 1. NO2* H,O CH;CO* cr OH- HBr NH3 Br2 b) Can you explain why y not select some of these?

Complete the following reactions by identifying the major organic product, reagents), or reactant. • If the product is a single compound, draw the structure clearly in the box. • List missing reagents neatly around the blue arrows. There may be more than one reagent per arrow. • If the product is a racemic mixture, clearly draw one enantiomer and write "racemic" under the answer.

Chemistry provide all major organic products. Please explain your answers!! H₂SO4 (cat.) H₂O reflux H₂SO4 (cat.) HO reflux

Which chloramine out of monochloramine (NH₂CL), dichloramine (NHCL₂) and trichloramine (NCL3) is the strongest oxidant. Please explain why?

Characterize EACH of the three given statements as being TRUE or FALSE and then indicate the collective true - false status of the statements using the choices. (1) Alcohols have higher boiling points than alkanes of similar molecular mass because of hydrogen bonding. (2) Polyols have similar boiling points to tertiary alcohols. (3) Primary and secondary alcohols give the same type of product when subjected to mild oxidizing agents. Group of answer choices All three statements are true. Two of the three statements are true. Only one of the statements is true. None of the statements are true.

(1) Determine the isometric relationship, constitutional, enantiomers, distereomers, geometric (cis/trans), or meso, between each pair of organic compounds. Please explain further than "identical" (ii) circle all structures that are not optically active. d. e. f.g. d. g. SH ļ SH SH SH Br 11 OH OH or or 3 SH z Br SH

https://drive.google.com/file/d/14UPPDWhJXm0KKcLAOXDyBULvI_sISzDW/view?usp=sharing Which hazard statement is false in regards to dichloromethane? 1) May be corrosive to metals 2) Causes skin irritation 3) Causes serious eye irritation 4) Suspected of causing cancer

Organic Chem.  This CANNOT be hand-drawn, explanation and illustrations must be typed or digital. if it is hand-drawn your answer will be incomplete and marked as wrong. Molecule: Benzocaine List and explain common industrial or medical applications. what ways can you synthesize this? identifyand discuss the differences. List out any specificprocedural details. Describe the theories behind any method used in asynthesis to create this molecule. (Reactions, techniques,instrumentation, etc.).■For example, if distillation could be used to purify your product, why.

1. Draw the chemical structures of both Amiodarone and Levothyroxine. Label all of the organic chemical reactions between them (you can use arrows, etc to do this). Aswell as explain Goitre in your own words, the increased iodine from the Amiodarone and why TSH may increase and T3, T4 remain normal etc. -0-CH2 -CH2-N Amiodarone C;H5 CH2)3 CH3 но NH2 Levothyroxine HO. HO. ÑH2