Structure 4: Draw the structure with a postively charged oxygen. H₂C X CH, H₂C CH3

Q: Why is H3C-O-SiH3 ether a weaker base than (CH3)3O?

A: due to Pπ-Pπ back bonding

Q: Draw an expanded structural formula of pent-1-en-3-yne/ CH3-CC-CH=CH2 and then label each carbon.…

A:

Q: Structure 3: Draw the structure with a positively charged carbon. Incorrect H₂C H₂C 01 CH₂ 0- CH₂…

A: Resonance structures are the collection of Lewis structures that represent the delocalisation of…

Q: Draw all the alkyl halides with molecular formula C 5H 11Cl formed when pentane (CH 3CH 2CH 2CH 2CH…

A: The monohalogen derivative of alkanes are usually reffered to as haloalkane or alkyl halide. They…

Q: Draw 2- methyl propyl

A: -yl subscript is used for the function groups of --alkyl( Cn H2n+1 ).

Q: 3. Complete the following reactions by drawing structures for the products in each case. NaOH SH Br…

A: Organic transformation

Q: Identify the structure that is not correct. O

A: This question is related to reaction intermediates. Reaction intermediates are of many types such as…

Q: COB ECH NaOEt/EtOH

A:

Q: Predict reagents needed to complete this E1 elimination reaction. Br

A: The formation of alkene from an alkyl halide in the present of a certain chemical reagent is called…

Q: Why is H3C-O-SİH3 ether a weaker base than (CH3)3O?

A:

Q: Rank the compounds according to the * ?increase in boiling point R-NH2 < R-OH < R-COOH O R-OH<…

A: Boiling point of the substance depends upon the inter-molecular force of attraction present in the…

Q: 6. Use arrow pushing to draw the product of the resulting reaction. If no reaction occurs, then…

A: Oxidation of alcohols is generally obtained from Chromic acid or KMnO4 as a reagent.

Q: + H CH3 H ::

A: Step 1:Complete reaction is given as :- Nucleophilic Attack: The chloride ion (Cl-)  acting as the…

Q: 1) 2 CH3MgBr 1) CH,MgBr Y Co,CH3 2) H20, HCI 2) Н,О, НCI

A: Given,

Q: Draw 3-methylcyclobutanol. Include all hydrogen atoms.

A:

Q: Chemistry J C6H5 enol form 0 Keto form C6H5 H keto form keto form please show electron arrow. II OH…

A: The keto–enol tautomerism describes the chemical equilibrium between a keto form (a ketone or an…

Q: explain why methanethiol, CH3SH, has a lower boiling point (6°C) than methanol, CH3OH (65°C), even…

A: Boiling point is the point at which liquid start to boil. Factor affecting the boiling point.…

Q: Identify the principal organic product in each case

A: In the given reaction the alcohol reacts with a base to form an alkoxide ion and the alkoxide ion…

Q: OH H3C Type of Reaction: CH3 CH3 _CH3 + OH Type of Reaction: + [0] НО

A: Organic reactions are given.

Q: Which compounds are acetals? || OH II IV O , I, II O I,I O II, I, IV O II, IV

A:

Q: Example: H 1 Ca R , coo (0 NH3 L or D?

A: 1) If the -NH2 group is present on the left, it is L-amino acid. 2) If the -NH2 group is present on…

Q: 1: Give at least five (5) uses of Alcohol and Phenol Name Functional Group Alcohols R-OH LOH Phenols…

A:

Q: What is the molecular geometry of the circled carbon? НО, ОН

A: Is that defined by the position of the atoms not the nonbonding pairs.Sp3 hybridization=&gt;…

Q: ОН 2 CHОН dry ÉCI H Ag(NH3)* NH,OH H* HCN OH

A:

Q: "H D Me H₂SO4, EtOH NaOEt, EtOH

A:

Q: for trans-1.2-dichlorocyo 3. The structure below is Formeterol, a long-acting b-adrenergic agonist…

A: Redraw the structure and label all the functional groups--

Q: 4. Draw 3 resonance structures for each framework, indicate all formal charges, and cirele preferred…

A: Here we have to write three resonance structures of the following frame work present in the molecule…

Q: Name each compound. CH; CH, CH, · CH3-CH-CH-CH-CEC-H CH3

A: The given compound is,

Q: Ni H +

A: In the given reaction, there is a double bond in the cyclic ring, thus, it is a cycloalkene. It is…

Q: H H The compound H– Ç–C▬C -0-C-H is an example of an H HH ether. O True O False

A: The given statement is, The compound CH3CH2CH2OCH3 is an example of an ether.   The given compound…

Q: 2) complete the reaction: CO,H SO3 H2SO4 NO2

A: Both nitro and carboxyl groups are meta directing groups. Hence sulphonation occurs at a position…

Q: HCI CH3OH

A: Given that, the reaction is: